Gene: HRAS ×
Source: CLINVAR ×
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: rs121913496
rs121913496
HRAS ; LRRC56
11 0.724 0.440 11 533873 missense variant C/A;G;T snv 0.700 1.000 2 1986 1991
dbSNP: rs28933406
rs28933406
HRAS ; LRRC56
17 0.667 0.480 11 533875 missense variant G/C;T snv 0.700 0