Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs7740107 1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs3795503 1 180936558 synonymous variant C/T snv 0.31 0.27 3
rs2412608 15 41204515 intron variant C/T snv 0.36 2
rs284316 1 10673024 intron variant T/C;G snv 2