Gene: HCCS ×
Source: ALL
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: rs193929392
rs193929392
ARHGAP6 ; HCCS
4 0.851 0.120 X 11118574 missense variant G/A snv 0.010 1.000 1 2007 2007