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: rs11795613
rs11795613
2 0.925 0.120 X 71147478 intron variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs4844285
rs4844285
2 0.925 0.120 X 71150394 intron variant G/A snv 0.010 1.000 1 2018 2018