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rs104894227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894227(A;G)
Make rs104894227(G;G)
ReferenceGRCh37 37.1/132
Chromosome11
Position533553
GeneHRAS
is asnp
is mentioned by
dbSNPrs104894227
ebirs104894227
HLIrs104894227
Exacrs104894227
Varsomers104894227
Maprs104894227
PheGenIrs104894227
hapmaprs104894227
1000 genomesrs104894227
hgdprs104894227
ensemblrs104894227
gopubmedrs104894227
geneviewrs104894227
scholarrs104894227
googlers104894227
pharmgkbrs104894227
gwascentralrs104894227
openSNPrs104894227
23andMers104894227
23andMe allrs104894227
SNP Nexus

SNPshotrs104894227
SNPdbers104894227
MSV3drs104894227
GWAS Ctlgrs104894227
Max Magnitude0
OMIM190020
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894227(G;G)
Alt rs104894227(G;G)
Reference rs104894227(A;A)
Significance Pathogenic
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.533553T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013439.24,