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rs104894231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894231(A;A)
Make rs104894231(A;G)
ReferenceGRCh37 37.1/132
Chromosome11
Position533467
GeneHRAS
is asnp
is mentioned by
dbSNPrs104894231
ebirs104894231
HLIrs104894231
Exacrs104894231
Varsomers104894231
Maprs104894231
PheGenIrs104894231
hapmaprs104894231
1000 genomesrs104894231
hgdprs104894231
ensemblrs104894231
gopubmedrs104894231
geneviewrs104894231
scholarrs104894231
googlers104894231
pharmgkbrs104894231
gwascentralrs104894231
openSNPrs104894231
23andMers104894231
23andMe allrs104894231
SNP Nexus

SNPshotrs104894231
SNPdbers104894231
MSV3drs104894231
GWAS Ctlgrs104894231
Max Magnitude0
OMIM190020
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894231(A;A)
Alt rs104894231(A;A)
Reference rs104894231(G;G)
Significance Pathogenic
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.533467C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013441.17,