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: rs1164509546
rs1164509546
ARHGEF7
1 1.000 0.040 13 111286234 missense variant C/T snv 4.0E-06 0.010 1.000 1 2004 2004