Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894808
rs104894808
4 0.851 0.120 X 48792376 missense variant G/T snv 0.700 0
dbSNP: rs104894815
rs104894815
9 0.776 0.120 X 48792337 missense variant G/A snv 0.700 0