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
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs2286276
TBL2
0.925 0.120 7 73573024 non coding transcript exon variant C/T snv 0.28 5
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 3
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 3
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 3
rs5996074
SREBF2
22 41840333 intron variant G/A snv 0.74 3
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 2
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 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
rs151181
CLN3
1.000 0.040 16 28479196 intron variant T/C snv 0.32 2
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 2
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 2
rs3781264
PLCE1
0.851 0.120 10 94310618 intron variant A/G snv 0.25 2
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 2
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 2