Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs121918324 0.925 0.160 1 161167187 missense variant C/T snv 3
rs767419411 0.882 0.200 1 161168069 missense variant G/A;C snv 1.2E-05; 8.0E-06 3
rs28934595 0.925 0.160 6 26091354 missense variant A/C snv 2
rs28936676 0.925 0.160 1 161170467 stop lost A/C snv 2
rs1227507479 1.000 0.160 6 26092783 missense variant T/C snv 4.0E-06 1
rs121918323 1.000 0.160 1 161169070 missense variant G/C snv 1
rs121918325 1.000 0.160 1 161168462 missense variant C/T snv 4.0E-06 1
rs121918326 1.000 0.160 1 161166906 missense variant A/C snv 1
rs1317835140 1.000 0.160 1 161167131 missense variant G/A snv 4.0E-06 1
rs141274934 1.000 0.160 1 161170711 missense variant C/A;G snv 4.0E-06 1
rs1558033572 1.000 0.160 1 161169903 splice acceptor variant TA/- del 1
rs369381477 1.000 0.160 1 161168072 missense variant G/A snv 4.0E-06 1
rs374936130 1.000 0.160 1 161170493 missense variant G/A;C snv 8.0E-06 1
rs41270025 1.000 0.160 1 161168463 missense variant G/A;T snv 1
rs751599052 1.000 0.160 1 161169025 missense variant C/A;T snv 4.0E-06; 6.4E-05 1
rs757473753 1.000 0.160 1 161168492 missense variant C/G snv 4.0E-06 7.0E-06 1
rs764352037 1.000 0.160 1 161167181 missense variant G/A snv 4.0E-06 1
rs769452432 1.000 0.160 1 161166892 missense variant G/T snv 1
rs776530007 1.000 0.160 1 161170724 missense variant A/C;T snv 4.0E-06; 4.0E-06 1
rs786204784 1.000 0.160 1 161167209 frameshift variant C/- delins 1
rs900431442 1.000 0.160 1 161170464 missense variant A/G snv 1
rs1361576529 1.000 0.160 1 161171039 missense variant G/C snv 1
rs928944841 1.000 0.160 1 161171099 missense variant G/A snv 7.0E-06 1