Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 14
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs77543610 0.667 0.560 10 121520160 missense variant G/C snv 12
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 8
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 6
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 4
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 4
rs28931615 0.732 0.240 4 1804426 missense variant C/A;T snv 3
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 3
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 3
rs9642880 0.776 0.240 8 127705823 intron variant G/A;T snv 3
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 2
rs10775480 0.882 0.120 18 45737317 intron variant T/C snv 0.61 2
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs17674580 0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 2
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 2
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 2
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 2
rs760805 0.776 0.240 1 24925432 intron variant A/T snv 0.42 2