Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs187269 0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs7597593 0.827 0.160 2 184668853 intron variant T/C snv 0.53 6