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: rs367665974
rs367665974
1 1.000 0.200 X 153870122 missense variant C/T snv 5.5E-06 0.700 1.000 20 1994 2017