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: rs137854587
rs137854587
1 1.000 0.120 X 37796092 missense variant C/T snv 0.800 1.000 20 1989 2016