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: rs945508
rs945508
ARHGEF11 ; LRRC71 ; MIR765
3 1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 0.010 1.000 1 2008 2008