Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10042590 5 88477501 intron variant G/A snv 5.8E-02 1
rs10850407 12 114940232 intergenic variant T/G snv 0.24 1
rs113602013 18 60252477 intergenic variant G/A;C snv 1
rs1149643 1 56163763 intron variant A/T snv 0.49 1
rs11605518 11 13248667 intergenic variant A/G snv 0.72 1
rs11826048 11 103527569 intergenic variant C/T snv 9.6E-02 1
rs12324159 15 41170270 regulatory region variant G/A snv 0.47 1
rs12358504 10 121240352 intergenic variant A/G snv 0.18 1
rs13021222 2 164191395 intron variant G/C;T snv 1
rs13265769 8 81912028 intron variant T/C snv 0.35 1
rs13358657 5 158511062 intron variant A/G snv 0.11 1
rs142076278 16 51794418 intergenic variant A/G snv 9.5E-03 1
rs150532297 5 158169198 downstream gene variant G/A snv 4.1E-03 1
rs1507151 6 78773529 intergenic variant T/C snv 0.32 1
rs17006217 3 19741785 intergenic variant T/A;C snv 1
rs2078339 12 20008234 intron variant A/G snv 0.28 1
rs2114820 10 86412952 intergenic variant G/A snv 0.39 1
rs221907 14 71129630 intergenic variant A/G snv 0.58 1
rs2246490 14 103517957 downstream gene variant G/T snv 0.67 1
rs2478981 20 63852557 intergenic variant T/G snv 0.57 1
rs271695 5 64440647 intron variant C/T snv 0.39 1
rs28711771 1 16093094 intergenic variant G/A snv 0.52 1
rs2872812 17 40602398 upstream gene variant G/A snv 0.60 1
rs2962383 5 158067851 intergenic variant C/T snv 0.28 1
rs2977324 8 75804502 intergenic variant T/G snv 0.77 1