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: rs727503093
rs727503093
HRAS ; LRRC56
2 0.925 0.160 11 533881 missense variant C/T snv 0.700 1.000 10 1982 2018