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: rs2762051
rs2762051
1.000 0.080 13 50261579 intron variant C/T snv 0.15
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.810 1.000 1 2010 2014
dbSNP: rs806321
rs806321
0.851 0.160 13 50267187 intron variant C/T snv 0.47
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 2 2011 2019
dbSNP: rs9596270
rs9596270
1.000 0.080 13 50268304 intron variant T/C snv 6.1E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs3118905
rs3118905
13 50531198 intron variant G/A snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 3 2010 2019
dbSNP: rs3118906
rs3118906
13 50532652 intron variant G/A snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 3 2013 2019
dbSNP: rs2812208
rs2812208
13 50132951 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs3116602
rs3116602
13 50537219 intron variant T/G snv 0.15
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2008 2019
dbSNP: rs41284828
rs41284828
13 50389549 non coding transcript exon variant G/A snv 2.3E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs797486
rs797486
13 50647482 intron variant C/A snv 0.85
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 2 2018 2019
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