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: rs128624223
rs128624223
2 0.925 0.160 X 153740147 missense variant C/T snv 0.010 1.000 1 1995 1995
dbSNP: rs973742
rs973742
2 0.925 0.160 1 158190738 downstream gene variant G/A snv 0.42 0.010 1.000 1 2012 2012