Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3792785
TNIP1
1.000 0.120 5 151072089 intron variant T/C snv 0.13 1
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 2
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs886403
MUC21
0.925 0.160 6 30989841 3 prime UTR variant T/C snv 0.23 2
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 2
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 1
rs4678
VARS2
0.925 0.200 6 30926164 missense variant G/A snv 0.14 0.15 2
rs887464
POU5F1 ; PSORS1C3
0.925 0.200 6 31178143 intron variant C/A;T snv 2
rs7749323 0.925 0.200 6 137909252 intergenic variant G/A snv 3.3E-02 1
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 3
rs3095089 0.882 0.240 6 30966017 upstream gene variant G/T snv 0.16 3
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 2
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4