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
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 6
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs919462
MAPT
0.807 0.120 17 45988374 intron variant C/T snv 0.15 6
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 5
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 5
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35 5
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 4