Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434282 1.000 0.080 1 75749552 missense variant G/C snv 4.0E-06 1
rs121434283 1.000 0.080 1 75733603 missense variant C/T snv 1.2E-05 1
rs1215335509 1.000 0.080 1 75750514 stop gained G/A;T snv 1
rs1225471006 1.000 0.080 1 75761173 stop gained -/TAGAATGAGTTAC delins 3.2E-05 2.8E-05 1
rs1227800781 1.000 0.080 1 75761231 missense variant A/G snv 7.0E-06 1
rs1319192670 1.000 0.080 1 75732688 frameshift variant T/- delins 7.0E-06 1
rs1325949559 1.000 0.080 1 75728417 frameshift variant C/- del 1
rs1348176225 1.000 0.080 1 75749427 missense variant C/A;G snv 1
rs1462472677 1.000 0.080 1 75762704 missense variant A/G;T snv 4.0E-06 1
rs148207467 1.000 0.080 1 75761221 stop gained C/A;T snv 4.0E-06 1
rs148260275 1.000 0.080 1 75740112 splice donor variant T/C snv 4.0E-06 7.0E-06 1
rs149678400 1.000 0.080 1 75745889 missense variant C/A;T snv 2.9E-04; 4.0E-06 1
rs1553121887 1.000 0.080 1 75724790 start lost G/C snv 1
rs1553122996 1.000 0.080 1 75732924 splice donor variant T/G snv 1
rs1553123857 1.000 0.080 1 75739978 splice acceptor variant A/C snv 1
rs1553124805 1.000 0.080 1 75745916 splice donor variant T/G snv 1
rs1553125211 1.000 0.080 1 75749417 splice acceptor variant A/C snv 1
rs1553125264 1.000 0.080 1 75749536 frameshift variant GCT/CC delins 1
rs1553127172 1.000 0.080 1 75761165 frameshift variant TTGAACTAGCTAGAATGAGTTA/- del 1
rs1553127216 1.000 0.080 1 75761366 missense variant A/C snv 1
rs1553127378 1.000 0.080 1 75762691 splice acceptor variant G/C snv 1
rs1557446524 1.000 0.080 1 75734857 stop gained G/T snv 1
rs1557457623 1.000 0.080 1 75749504 stop gained GTGACGGAGC/TTTAA delins 1
rs1557466604 1.000 0.080 1 75761126 missense variant A/T snv 1
rs200724875 1.000 0.080 1 75745823 missense variant G/A;T snv 1.6E-05 1