Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs760077 0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs9472135 0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11072567 15 76006403 intron variant A/G snv 0.43 5
rs128494 21 36461960 intron variant T/C snv 0.72 4
rs2878889 18 48936766 intron variant A/C;G;T snv 2