Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 3
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 2
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 1
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 1
rs1679013 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 1
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 1
rs35748167 1.000 0.120 18 60370200 intron variant G/C;T snv 1
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 1
rs4368253 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 1
rs674313 0.925 0.120 6 32610305 intergenic variant C/T snv 0.29 1
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 1
rs8024033 0.925 0.120 15 40111456 upstream gene variant C/G snv 0.50 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 1
rs1439287
ACOXL-AS1 ; ACOXL ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs4987852
BCL2
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02 1
rs4987855
BCL2
0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02 1
rs4987856
BCL2
0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02 1
rs6858698
CAMK2D
0.925 0.120 4 113762688 upstream gene variant G/C snv 0.20 1
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2