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rs121917756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917756(A;A)
Make rs121917756(A;G)
ReferenceGRCh37.p5 37.3/135
Chromosome11
Position533869
GeneHRAS
is asnp
is mentioned by
dbSNPrs121917756
ebirs121917756
HLIrs121917756
Exacrs121917756
Varsomers121917756
Maprs121917756
PheGenIrs121917756
hapmaprs121917756
1000 genomesrs121917756
hgdprs121917756
ensemblrs121917756
gopubmedrs121917756
geneviewrs121917756
scholarrs121917756
googlers121917756
pharmgkbrs121917756
gwascentralrs121917756
openSNPrs121917756
23andMers121917756
23andMe allrs121917756
SNP Nexus

SNPshotrs121917756
SNPdbers121917756
MSV3drs121917756
GWAS Ctlgrs121917756
Max Magnitude0
OMIM190020
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121917756(A;A)
Alt rs121917756(A;A)
Reference rs121917756(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene HRAS
CLNDBN Myopathy, congenital, with excess of muscle spindles
Reversed 1
HGVS NC_000011.9:g.533869C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013442.23,