In Japanese, 6.2x increased risk of developing prostate cancer, a 3x increased risk of developing BPH, and a 5.5x increased risk of developing metastatic prostate cancer see discussion at rs2011077
A study of ~500 Japanese prostate cancer patients found that individuals with a rs2011077(G;G) genotype had a 6.2- and 3-fold increased risk of prostate cancer and benign prostate hyperplasia (BPH), and a 5.5-fold increased risk of metastatic prostate cancer, compared to the (A;A) genotype.
more info
Bad
3
64.6%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2015-12-01
0.2493
1
FGFR4
5
177094455
3
2018-12-06
minus
minus
Prostate cancer
1.3x to 11.5x Increased risk of autoimmune thyroid disease The 1.3x risk was for carriers of the minor allele in a Caucasian population. The 11.5x risk was for heterozygotes (GT only) in the Han Chinese population in a 2015 study. See text at rs180223
A 2015 research study titled "Correlation between thyroglobulin gene polymorphisms and autoimmune thyroid disease" focused on the Han Chinese population. A total of 270 patients with AITD and 135 healthy controls were enrolled. They found "The Tg SNP frequency distribution was significantly different between Han populations of the Northern regions of Henan province and the Xi'an regions of Shaanxi province" (Abstract).
•Separate ODs were found for the following TG gene SNPs:

•E10SNP24 T/G rs180223 = TT 1.35, TG 11.50, GG 0.14, (TG OD was 95%CI = 4.89-27.06, p=<0.01)

•E10SNP158 T/C rs2069550 = TT 1.07, TC 0.96, CC 1.03

•E12SNP A/G rs853326 = AA 0.51, AG 0.23, GG 4.22 (GG OD was 95%CI = 2.65-6.73, p=<0.01)

•E33SNP C/T rs2076740 = CC 1.11, CT 0.93, TT 0.98....
more info
Bad
2.8
49.6%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2018-01-17
0.36
Other
2
TG
8
132888007
2.8
2018-12-06
plus
plus
Graves' disease
Slow metabolizer of certain substances see Gs310 Being a slow metabolizer of certain substances
Bad
2.7
2019-03-22
probably light-skinned, European ancestry This SNP influences skin pigmentation and indicates indicates light-skinned European ancestry. estimates that the rs1426654(A) allele (light skin pigmentation) spread through the European population around 6,000 - 12,000 years ago. Prior to that, "European ancestors" were most likely relatively brown-skinned.
This SNP influences skin pigmentation. The allele, A111T, rs1426654(A), indicates light-skinned West Eurasian ancestry. [, ] It appears as if this SNP is a relatively new one in human evolution; one estimate is that the rs1426654(A) allele, in other words, light skin pigmentation, spread through the European population around 6,000 - 12,000 years ago. Prior to that, "European ancestors" were most likely relatively brown-skinned. Another study () has concluded that almost individuals carrying the A111T variant can trace ancestry back to a single person who most likely lived at least 10,000 years ago. This SNP is one of three from the SLC24A5 gene that can be analyzed to categorize the ancestry of a person as either West Eurasian (Middle Eastern, Caucasian, European, etc.), African, or East Eurasian, based on a 2009 study....
more info
2.7
100%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2011-08-12
0.4775
Other
18
MYEF2 SLC24A5
15
48134287
2.7
2018-12-06
plus
plus
Lower heart attack risk than average You are in the ~30 % of people (depending on the population studied) who carry two minor alleles at two SNPs, rs1108580 and rs1611115. This genoset is reported as having 0.59x the risk of a heart attack or cardiovascular incident compared to people who carry zero of the minor alleles for these two SNPs, based on a study of 3,000 African-Americans enrolled in the Jackson Heart Study.
Good
2.6
2015-02-12
claimed to be part of the 12% of the population who can lose weight with any type of exercise An interesting hypothesis, but not well validated, this patent is summarized in a simplified blog post and suggests a genotype to suggest diet and lifestyle changes which may be beneficial. based on rs4994(T;T) and rs1042713(A;A)
Good
2.5
2016-04-21
Higher risk for number of cancers
600+ Korean lung cancer patients were part of a study that concluded that the rs664143(T) allele, as oriented vis-a-vis dbSNP, located in the ATM gene and also known as IVS62+60G>A, was associated with increased risk, with an odds ratio of 1.68 (CI: 1.1-2.1, p<0.05). In a study of 119 American patients with potentially resectable pancreatic cancer, the rs664143(C) allele was associated with poorer overall survival (ie response) to combined gerncitabine radiation therapy. Also, as 1 of 3 SNPs its risk allele is associated with poorer overall survival for pancreatic cancer patients being treated with combined gerncitabine radiation therapy; median overall survival times of 31.0, 16.2, and 10.5 months were calculated for pancreatic cancer patients carrying < or = 1, 2, and 3 risk alleles from...
more info
Bad
2.5
54%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2015-05-24
0.404
12
ATM C11orf65
11
108354934
2.5
2018-12-06
minus
minus
Lung cancer Pancreatic cancer
increased risk of myopia
[GWAS:Myopia (pathological)]
more info
Bad
2.5
9.5%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2014-02-08
0.1442
1
CNTN5
11
100172688
2.5
2018-12-06
plus
plus
increased risk of baldness
Baldness paper from 23andMe June 2012
more info
Bad
2.5
15%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2013-11-06
0.4444
1
HDAC9
7
18838251
2.5
2018-12-06
plus
plus
NatGeo
Baldness
slightly (17%) higher risk of colorectal cancer correlated with consumption of processed meats
rs4143094 is a SNP identified by a genome-wide diet-gene interaction analysis (GxE), and was found to be associated with increased risk of colon cancer correlated to the dietary variable of processed meat consumption. It is located on chromosome 10p14, 7.2kb upstream of GATA binding protein 3 (GATA3), in the promoter region of the gene rs4143094 was identified in a screen of 2.7 million SNPs for the risk of colorectal cancer, by combining 10 studies comparing 9287 cases and 9117 controls. Data was obtained from the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) and analyzed by conventional case-control logistic regression for multiplicative interactions between SNPs and dietary factors. rs4143094 was the most significantly implicated SNP in 10p14 for processed meat consumption linked with occurrence of...
more info
Bad
2.5
35.4%
TSIMKKMEXLWKGIHCHDASWYRIJPTHCBCEU0255075100
2015-11-03
13
GATA3
10
8047173
3.1
2018-12-06
plus
plus
Colorectal cancer

ABO blood group predictions are brand new, and still under development. We're rolling it out to you so we can see how it performs on real data. All conclusions are still greatly limited by the general lack of phased data, the lack of genotyping at all of the necessary snps, and other factors.

best guess:

ABO blood type
unknown(Rh unknown)

while your prediction is based on your phased data, explanations aren't yet available for phased data. I can offer this explanation taken from the unphased prediction which suggests blood type: unknown
you were not genotyped at rs8176719 so it is impossible to see type-O. This is a MAJOR limitation of your data
can't reliably identity type-A without rs8176746 and rs8176747. can't reliably identity type-B without rs8176746 and rs8176747. neither rs8176747 nor rs8176746 supplied. impossible to determine type-A. neither rs8176747 nor rs8176746 supplied. impossible to determine type-B
you were not genotyped at either rs590787 nor i4001527 so it is impossible to see your Rh blood type

But the ABO system is quite limited

Blood, you see, doesn't just come in types A, B, AB, and O. The "positive" or "negative?" Nope. In fact, let's get all the way into the weeds: Scientists have since discovered over 300 proteins that contribute to blood type. The AB+ on your blood donor card? Yeah, that's a massive oversimplification... read more at Beyond Blood Type: Genomics Can Show What You're Really Made Of

or

It would be straightforward if we all had the same blood. But we don't. On the surface of every one of our red blood cells, we have up to 342 antigens - molecules capable of triggering the production of specialised proteins called antibodies. It is the presence or absence of particular antigens that determines someone's blood type.

Some 160 of the 342 blood group antigens are 'high-prevalence', which means that they are found on the red blood cells of most people. If you lack an antigen that 99 per cent of people in the world are positive for, then your blood is considered rare. If you lack one that 99.99 per cent of people are positive for, then you have very rare blood.

If a particular high-prevalence antigen is missing from your red blood cells, then you are 'negative' for that blood group. If you receive blood from a 'positive' donor, then your own antibodies may react with the incompatible donor blood cells, triggering a further response from the immune system. These transfusion reactions can be lethal. Read more at The man with the golden blood.

Known ABO SNPs

23andMe ABO
IndexGeneSNPGenoReputeMagnitudeSummary
1   rs7466519 not tested
2   rs8176750 not tested
3   rs56202119 not tested
4   i4000505 not tested
5   rs56231718 not tested
6   rs55788852 not tested
7   rs55927860 not tested
8   rs8176749 (G;G)   0
9   rs56190619 not tested
10   rs55783488 not tested
11   rs56355240 not tested
12   i4000504 not tested
13   rs56409303 not tested
14   rs55805279 not tested
15   rs56106480 not tested
16   rs8176747 not tested
17   rs41302905 (C;C) Good 0 common in complete genomics
18   rs8176746 not tested
19   rs8176745 not tested
20   rs55951833 not tested
21   rs8176743 (G;G)   0
22   i5007173 not tested
23   rs55739900 not tested
24   rs56116432 not tested
25   rs56031507 not tested
26   rs8176741 not tested
27   rs56408700 not tested
28   rs8176740 not tested
29   rs55827808 not tested
30   rs8176739 not tested
31   rs56223957 not tested
32   rs56189011 not tested
33   rs56089890 not tested
34   rs55727303 not tested
35   rs7853989 (G;G)     Not blood group B
36   rs55964869 not tested
37   rs55756402 not tested
38   i5007171 not tested
39   rs1053878 (C;C) Good 0 common in complete genomics
40   rs55658842 not tested
41   rs7873522 not tested
42   rs8176732 not tested
43   rs2073824 (A;A)    
44   rs8176722 (G;G)    
45   rs8176721 not tested
46   rs8176720 not tested
47   rs8176719 not tested
48   rs56231711 not tested
49   rs8176717 not tested
50   rs512770 (G;G)    
51   rs641959 not tested
52   rs514708 not tested
53   rs55958637 not tested
54   rs549446 not tested
55   rs8176704 (C;C)    
56   rs574347 (T;T)    
57   rs688976 not tested
58   rs687289 (C;C)    
59   rs2073828 not tested
60   rs55876802 not tested
61   rs8176694 (A;A)    
62   rs672316 not tested
63   rs657152 not tested
64   rs8176682 not tested
65   rs474279 not tested
66   rs500498 not tested
67   rs505922 not tested
68   rs507666 not tested
69   rs630014 (T;T)    
SNPedia ABO
IndexGeneSNPGenoReputeMagnitudeSummary
1   rs1053878 (C;C) Good 0 common in complete genomics
2   rs2073824 (A;A)    
3   rs2073828 not tested
4   rs2519093 not tested
5   rs41302905 (C;C) Good 0 common in complete genomics
6   rs500498 not tested
7   rs505922 not tested
8   rs507666 not tested
9   rs512770 (G;G)    
10   rs514659 not tested
11   rs55722397 not tested
12   rs55964869 not tested
13   rs56392308 not tested
14   rs574347 (T;T)    
15   rs612169 not tested
16   rs630014 (T;T)    
17   rs643434 not tested
18   rs644234 not tested
19   rs657152 not tested
20   rs687289 (C;C)    
21   rs687621 not tested
22   rs7853989 (G;G)     Not blood group B
23   rs8176694 (A;A)    
24   rs8176704 (C;C)    
25   rs8176719 not tested
26   rs8176720 not tested
27   rs8176722 (G;G)    
28   rs8176740 not tested
29   rs8176741 not tested
30   rs8176743 (G;G)   0
31   rs8176746 not tested
32   rs8176747 not tested
33   rs8176749 (G;G)   0
34   rs8176750 not tested
1
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