Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557863430 1.000 0.040 1 151405229 missense variant T/C snv 1
rs1557863440 1.000 0.040 1 151405233 missense variant T/C snv 1
rs1557863546 1.000 0.040 1 151405263 missense variant T/A snv 1
rs1557867853 1.000 0.040 1 151406330 missense variant G/A snv 1
rs1557870645 1.000 0.040 1 151407271 missense variant C/T snv 1
rs1557874046 1.000 0.040 1 151408807 missense variant T/G snv 1
rs1557901347 1.000 0.040 1 151424027 missense variant G/C snv 1
rs1557902023 1.000 0.040 1 151424154 missense variant G/C snv 1
rs1557909572 1.000 0.040 1 151427931 missense variant G/C snv 1
rs1557909821 1.000 0.040 1 151427999 missense variant A/G snv 1
rs1557910728 1.000 0.040 1 151428233 missense variant T/C snv 1
rs1557911386 1.000 0.040 1 151428357 missense variant T/A snv 1
rs1557916296 1.000 0.040 1 151430822 missense variant C/A snv 1
rs1557935477 1.000 0.040 1 151440939 missense variant G/T snv 1
rs1561824498 1.000 0.040 5 88752044 splice acceptor variant C/A snv 1
rs1564801388 1.000 0.040 10 87864353 5 prime UTR variant -/G delins 1
rs1564801473 1.000 0.040 10 87864406 5 prime UTR variant -/C delins 1
rs1564950387 1.000 0.040 11 687909 splice donor variant A/C snv 1
rs1565527302 1.000 0.040 11 70485988 frameshift variant TG/- del 1
rs1565532385 0.925 0.080 11 118374964 frameshift variant CA/- del 3
rs1567533189 0.925 0.160 16 2086283 frameshift variant AAGGACTGCCA/- del 2
rs1569305431 1.000 0.040 X 53254702 frameshift variant G/- delins 1
rs1569513495 1.000 0.040 22 50465238 stop gained C/A snv 1
rs16835979 0.851 0.120 4 4633549 intron variant C/A snv 0.20 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1