Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1149833
rs1149833
0.925 0.160 13 50176740 intron variant A/T snv 0.47
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs1149833
rs1149833
0.925 0.160 13 50176740 intron variant A/T snv 0.47
CUI: C0339471
Disease: Maculopathy with diabetes mellitus
Maculopathy with diabetes mellitus
0.700 1.000 1 2019 2019
dbSNP: rs117496431
rs117496431
13 50561606 intron variant C/T snv 8.5E-03
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs11842790
rs11842790
13 50350312 intron variant C/T snv 6.0E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs123378
rs123378
1.000 0.080 13 50514673 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs1239704
rs1239704
13 50578475 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
13 50532386 intron variant A/T snv 0.59
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs12429206
rs12429206
13 50871978 intron variant A/G snv 0.62
Prostate specific antigen measurement
0.700 1.000 1 2017 2017
dbSNP: rs1262720
rs1262720
13 50610289 intron variant G/A;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs12853498
rs12853498
13 50339738 intron variant T/A snv 5.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs12871645
rs12871645
13 50357429 intron variant G/T snv 3.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs12874278
rs12874278
13 50361786 intron variant C/T snv 6.5E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs12874827
rs12874827
13 50326600 intron variant T/G snv 5.5E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs143794540
rs143794540
13 50277750 intron variant A/G snv 5.4E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1568672
rs1568672
13 50179268 intron variant T/A snv 0.13
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs157170
rs157170
13 50508319 intron variant A/G snv 0.71
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs1638703
rs1638703
1.000 0.040 13 50514220 intron variant G/C snv 0.27
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.700 1.000 1 2018 2018
dbSNP: rs1638703
rs1638703
1.000 0.040 13 50514220 intron variant G/C snv 0.27
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms
0.700 1.000 1 2018 2018
dbSNP: rs17074093
rs17074093
13 50314567 intron variant A/G snv 5.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs17074143
rs17074143
13 50348637 intron variant A/T snv 5.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs17074145
rs17074145
13 50355253 intron variant G/C snv 5.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs17363566
rs17363566
13 50360756 intron variant G/A snv 6.5E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2018 2018
dbSNP: rs201798
rs201798
13 50380585 intron variant G/A snv 0.52
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019