Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 4
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 1
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 3
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 3
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 1
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 2
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 1
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 1
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7