Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs10069554 5 33204354 intron variant T/C snv 0.45 1
rs10279895 7 27288591 intergenic variant A/G snv 2.9E-02 1
rs11020821 11 94538497 intergenic variant C/A snv 0.28 1
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 1
rs145054295 11 96709521 intron variant AT/- del 7.0E-03 1
rs180912 10 113982069 regulatory region variant T/G snv 0.56 1
rs2469997 8 119341027 intergenic variant G/C snv 0.83 1
rs2820037 1.000 0.040 1 239273242 intergenic variant A/T snv 0.21 1
rs35434 12 115116871 intergenic variant G/A snv 0.22 1
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 1
rs7526425 1 211527316 regulatory region variant G/A snv 1
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 1
rs9375459 6 126826559 intron variant C/T snv 0.39 1
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 1
rs2992257
APBB1IP
10 26445658 intron variant C/T snv 0.20 1
rs6590812
ARHGAP42
11 100711497 intron variant G/A snv 0.55 1
rs11105368
ATP2B1
12 89680664 intron variant G/A;C snv 1
rs7297206
ATP2B1
12 89625452 intron variant C/A;T snv 1
rs148636776
ATXN2 ; SH2B3
0.790 0.280 12 111447491 missense variant G/A snv 1.5E-04 2.4E-04 1
rs28404156
BST1
4 15736109 missense variant G/A snv 7.4E-02 0.10 1
rs12715461
CACNA1D
3 53544856 intron variant A/C;G;T snv 1
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 1