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: rs2106809
rs2106809
8 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2008 2008
dbSNP: rs6632677
rs6632677
4 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1.000 1 2008 2008