Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs4646776
ALDH2
0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03 2
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 2
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 2
rs2238149
CCDC63
1.000 0.040 12 110874125 intron variant T/C snv 0.33 2
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 2
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2
rs4766526 1.000 0.040 12 110963512 downstream gene variant G/T snv 0.51 1
rs991817 1.000 0.040 12 110972733 intergenic variant A/G snv 0.62 1
rs10774610
CCDC63
1.000 0.040 12 110902439 intron variant T/C snv 0.36 1
rs11065733
CCDC63
1.000 0.040 12 110856716 intron variant A/G snv 0.57 1
rs11612727
CCDC63
1.000 0.040 12 110876485 intron variant T/C snv 0.31 1
rs2157876
CUX2
1.000 0.040 12 111154576 intron variant G/T snv 7.7E-02 1
rs4766542
CUX2
1.000 0.040 12 111152688 intron variant T/C snv 0.29 1
rs4766549
CUX2
1.000 0.040 12 111180528 intron variant T/G snv 0.17 1
rs4766553
CUX2
1.000 0.040 12 111196477 intron variant T/A;G snv 1
rs4766559
CUX2
1.000 0.040 12 111229180 intron variant C/T snv 0.22 1
rs4766567
CUX2
1.000 0.040 12 111269752 intron variant G/A snv 0.21 1
rs6490029
CUX2
0.925 0.120 12 111260653 intron variant G/A snv 0.36 1
rs7959625
CUX2
1.000 0.040 12 111185334 intron variant A/G snv 0.33 1
rs4766521
LINC01405
1.000 0.040 12 110949157 intron variant T/C snv 0.51 1