Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 1
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3