Source: GWASDB ×
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 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 2
rs1114832
PPP1R37 ; MARK4
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 2
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
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 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 2
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3