Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs387906517 0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448 0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913461 0.851 0.120 9 130862970 missense variant T/C snv 5
rs1057519773 0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451 0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913452 0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1057519771 1.000 0.080 9 130872201 missense variant G/C snv 2
rs121913454 0.925 0.080 9 130874969 missense variant A/G snv 2
rs121913460 0.925 0.080 9 130862971 missense variant A/T snv 2
rs1314838108 0.925 0.160 9 130854977 missense variant G/A snv 7.0E-06 2
rs1057519758 1.000 0.080 9 130872153 missense variant T/G snv 1
rs1057519772 1.000 0.080 9 130872895 missense variant A/G snv 1
rs1057519774 1.000 0.080 9 130872902 missense variant T/G snv 1
rs1057519775 1.000 0.080 9 130873028 missense variant T/G snv 1
rs1064156 1.000 0.080 9 130878519 missense variant G/A snv 4.0E-06 1
rs121913449 1.000 0.080 9 130862977 missense variant A/T snv 1
rs121913450 1.000 0.080 9 130873016 missense variant A/G snv 1
rs121913453 1.000 0.080 9 130862962 missense variant G/A snv 1
rs121913455 1.000 0.080 9 130862955 missense variant C/G snv 1
rs121913456 1.000 0.080 9 130862943 missense variant A/G snv 1
rs121913457 1.000 0.080 9 130873004 missense variant T/C snv 1
rs121913458 1.000 0.080 9 130862969 missense variant G/C;T snv 1
rs34549764 1.000 0.080 9 130862953 missense variant A/G snv 2.6E-03 2.5E-03 1