Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs4846204
KIF1B
1 10248900 intron variant C/T snv 9.3E-02 2
rs111604275
SUFU
10 102506502 intron variant C/T snv 3.7E-02 1
rs230525
NFKB1
0.882 0.080 4 102537720 non coding transcript exon variant G/A snv 0.69 1
rs7158166
TRAF3
14 102775462 upstream gene variant T/C snv 0.47 1
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 2
rs2679745
AZIN1-AS1 ; AZIN1
8 102864097 5 prime UTR variant G/A;C snv 1
rs117849885 11 103020694 intergenic variant A/C snv 1.5E-02 1
rs2288789
MACIR
5 103264823 intron variant G/A snv 0.31 2
rs117288711 8 103390144 intergenic variant C/A snv 5.2E-02 1
rs12885878 14 103541218 downstream gene variant A/G snv 0.71 1
rs2860284
CAND1.11 ; AMPD3
11 10364929 intron variant T/C snv 0.73 1
rs12879697
PPP1R13B
14 103806421 intron variant G/A snv 1.3E-02 1
rs61863693
LOC102724351
10 103960975 intergenic variant G/A snv 0.24 1
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10137527 14 105134327 intron variant C/T snv 8.3E-02 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs11850055
BRF1
14 105288195 intron variant T/C snv 0.30 1
rs9937170
EMP2
16 10531048 3 prime UTR variant T/C snv 0.50 1
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs3752246
ABCA7
1.000 0.080 19 1056493 missense variant G/C;T snv 0.84; 4.1E-06 2
rs7828
JAG1
20 10638366 3 prime UTR variant A/C snv 0.27 1
rs6484437
MRVI1
11 10645728 intron variant A/G;T snv 1
rs7766720
LINC02532
6 106725104 non coding transcript exon variant T/C snv 0.16 3
rs5745297
DAP
5 10680885 missense variant G/A snv 5.5E-02 5.7E-02 2