Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 2
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 1
rs221780 1.000 0.040 7 100699412 regulatory region variant G/C;T snv 1
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs13096071 1.000 0.040 3 101082799 intergenic variant T/A;C snv 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs6878284
SLCO6A1
0.925 0.040 5 102434022 intron variant C/T snv 0.64 1
rs1502844 1.000 0.040 5 102523613 regulatory region variant C/T snv 0.66 1
rs7085104
BORCS7-ASMT ; AS3MT
1.000 0.040 10 102869116 intron variant A/G snv 0.35 1
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 1
rs1046778
AS3MT ; BORCS7-ASMT ; LOC107984265
0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 1
rs7897654
LOC107984265
1.000 0.040 10 102902701 intron variant T/C snv 0.30 1
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 2
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs7775385 1.000 0.040 6 103198419 intergenic variant G/A;T snv 1
rs11191732
NEURL1
1.000 0.040 10 103572004 intron variant G/A snv 0.14 1
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 1
rs313327
CHST11
1.000 0.040 12 104580243 intron variant C/T snv 0.75 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 1
rs11952719 1.000 0.040 5 106755127 regulatory region variant C/T snv 0.45 1
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 1
rs1379552
STARD4-AS1
1.000 0.040 5 111643461 intron variant T/C snv 0.27 1
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7