Source: CURATED ×
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
rs10496288 2 83065441 intergenic variant T/C snv 0.13 1
rs10496289 2 83066256 intergenic variant C/T snv 0.13 1
rs11020821 11 94538497 intergenic variant C/A snv 0.28 1
rs12522034 5 36425491 intergenic variant G/A;C;T snv 1
rs145054295 11 96709521 intron variant AT/- del 7.0E-03 1
rs1656930 1.000 0.080 3 186835068 intergenic variant A/G snv 0.86 1
rs180912 10 113982069 regulatory region variant T/G snv 0.56 1
rs2447182 8 119341744 intergenic variant A/G snv 0.83 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
rs4463623 1 188331737 intergenic variant C/T snv 0.29 1
rs4977950 9 24732484 intergenic variant G/C;T snv 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
rs7542235 1.000 0.040 1 196854483 intron variant A/G snv 0.23 1
rs7735940 5 36423829 regulatory region variant G/T snv 0.65 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
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 1
rs2148582
AGT
1 230714053 intron variant A/G snv 0.58 1