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: rs137853265
rs137853265
2 0.925 0.200 X 54467901 missense variant C/T snv 7.9E-06 9.5E-06 0.010 1.000 1 2005 2005