Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 4
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 3
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 3
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 3
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 3
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 3
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 3
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 3
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 3
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 2
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 2
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs11199914 0.925 0.080 10 121334387 intergenic variant C/T snv 0.40 2
rs11242675 0.925 0.080 6 1318643 downstream gene variant C/T snv 0.58 2
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 2
rs11820646 0.925 0.080 11 129591276 upstream gene variant T/C;G snv 2
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 2