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: rs121918544
rs121918544
7 0.821 0.179 14 24240635 missense variant C/T snp 0.010 1.000 1 2009 2009
dbSNP: rs28936072
rs28936072
5 0.821 0.393 X 154765472 missense variant T/C snp 0.010 1.000 1 2003 2003