Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 4
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 2
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2
rs10774610
CCDC63
1.000 0.040 12 110902439 intron variant T/C snv 0.36 1
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 1