Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12