Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114208039
HLA-B ; HLA-C
6 31273862 intron variant A/G snv 2
rs115007843
SCD5
4 82654059 intron variant A/C snv 0.18 2
rs115340020
RPAP2 ; GLMN
1 92300881 intron variant G/A snv 1.7E-02 2
rs1157008 9 88920798 regulatory region variant T/C;G snv 3
rs11580646
TENT5C
1 117619797 intron variant C/G snv 0.14 2
rs11611647 12 4224753 intergenic variant T/C snv 0.22 3
rs11640143 16 85955858 regulatory region variant T/C;G snv 2
rs11642657 16 85982722 intron variant C/A;T snv 3
rs11686139 2 226426699 intergenic variant A/C snv 0.13 2
rs11723763
GYPA ; LOC107986317
4 144137143 intron variant G/T snv 0.36 2
rs117424492 15 79975053 upstream gene variant G/C;T snv 2
rs117533700
NFIX
19 13065914 intron variant C/G;T snv 2
rs11775706 8 6843366 intron variant C/G;T snv 2
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs11992162 8 11979005 upstream gene variant G/A;C;T snv 2
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs12149363 16 85895099 upstream gene variant C/G snv 7.9E-02 2
rs12151289 19 33260946 intergenic variant G/A;C;T snv 3
rs12232384 16 85976154 intron variant C/A;T snv 2
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs12312487
CMKLR1
12 108327859 intron variant G/A snv 0.31 2
rs12346772
LOC105376219
9 111158319 intron variant A/G snv 0.18 2
rs12458462
CTDP1
18 79712436 intron variant C/A snv 0.30 2
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19 3
rs12461821
TNFSF14
19 6671358 upstream gene variant G/A;C;T snv 2