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: rs104894229
rs104894229
HRAS ; LRRC56
73 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 0
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
73 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 0
dbSNP: rs121917756
rs121917756
HRAS ; LRRC56
2 0.925 0.120 11 533869 missense variant C/T snv 0.700 0
dbSNP: rs121917757
rs121917757
HRAS ; LRRC56
4 0.851 0.200 11 534259 stop gained G/A;T snv 1.2E-05 0.700 0