Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43