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: rs28935472
rs28935472
1 1.000 0.080 X 154360233 missense variant C/T snv 0.800 1.000 2 2003 2016
dbSNP: rs80338837
rs80338837
1 1.000 0.080 X 154360243 missense variant G/T snv 0.700 1.000 2 2003 2016