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: rs104894914
rs104894914
4 0.851 0.120 X 154191716 missense variant T/C snv 0.810 1.000 2 1995 2012
dbSNP: rs267606927
rs267606927
2 0.925 0.120 X 154190173 missense variant T/C snv 0.700 1.000 1 2010 2010