Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5
rs3117426
LOC105375005 ; OR14J1
0.925 0.080 6 29304235 intron variant C/T snv 0.21 2
rs1012507
TNFSF4 ; LOC100506023
1.000 0.080 1 173250332 intergenic variant G/T snv 0.32 1
rs10156091
ICA1
1.000 0.080 7 8147464 intron variant T/C snv 0.86 1
rs10239340
TNPO3
1.000 0.080 7 129028456 intron variant T/A;G snv 1
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 1
rs10279821
TNPO3
1.000 0.080 7 129043493 intron variant T/A;C snv 1
rs10466455
LOC102723568
1.000 0.080 11 34759389 intergenic variant T/C snv 0.39 1
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs10798269
TNFSF4 ; LOC100506023
1.000 0.080 1 173340574 intergenic variant A/G;T snv 1
rs10845606
GPR19
1.000 0.080 12 12681960 intron variant C/A snv 0.15 1
rs10903340 1.000 0.080 8 11593078 regulatory region variant T/A;C;G snv 1
rs10911628 1.000 0.080 1 184680369 intergenic variant C/A snv 9.4E-02 1
rs10946940 1.000 0.080 6 27592808 upstream gene variant A/C;G snv 1
rs11073328
FAM98B
1.000 0.080 15 38472642 intron variant C/T snv 9.3E-02 1
rs1133906
SAMD9L
0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 1
rs1143678
ITGAM
1.000 0.080 16 31331684 missense variant C/T snv 0.15 0.17 1
rs1143683
ITGAM
1.000 0.080 16 31325567 missense variant C/T snv 0.16 0.16 1
rs11655550 1.000 0.080 17 39453870 upstream gene variant T/C snv 0.16 1
rs1167796
HIP1
1.000 0.080 7 75543861 intron variant G/A snv 0.32 1
rs1167797
HIP1
1.000 0.080 7 75546611 intron variant C/A;T snv 1
rs11697848 1.000 0.080 20 49958778 downstream gene variant C/T snv 3.6E-02 1
rs11783247
XKR6
1.000 0.080 8 10931365 intron variant C/T snv 0.54 1
rs12537284 1.000 0.080 7 129077852 intergenic variant G/A snv 0.11 1