Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1556022962 X 133304782 missense variant C/T snv 1
rs1048369 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs1556022641 1.000 0.200 X 133303022 stop gained G/A snv 1
rs1556022644 1.000 0.200 X 133303052 stop gained C/A snv 1
rs1556025980 1.000 0.200 X 133324154 frameshift variant -/T delins 1
rs1556028269 1.000 0.200 X 133339186 frameshift variant C/- del 1
rs1569339879 1.000 0.200 X 133303016 frameshift variant -/GCAC delins 1
rs1569341521 1.000 0.200 X 133311393 frameshift variant G/- delins 1