Gene: HRAS ×
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: rs104894228
rs104894228
HRAS ; LRRC56
48 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 3 2006 2018
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
73 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs1434040739
rs1434040739
HRAS ; LRRC56 ; LOC101059906
2 0.925 0.200 11 532745 missense variant T/A snv 8.1E-06 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs878854761
rs878854761
HRAS ; LRRC56
1 1.000 0.160 11 534319 missense variant T/C snv 0.010 1.000 1 2012 2012