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rs398122809

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122809(-;-)
Make rs398122809(-;AGA)
Make rs398122809(AGA;AGA)
ReferenceGRCh37.p10 37.5/138
Chromosome11
Position534212
GeneHRAS
is asnp
is mentioned by
dbSNPrs398122809
ebirs398122809
HLIrs398122809
Exacrs398122809
Varsomers398122809
Maprs398122809
PheGenIrs398122809
hapmaprs398122809
1000 genomesrs398122809
hgdprs398122809
ensemblrs398122809
gopubmedrs398122809
geneviewrs398122809
scholarrs398122809
googlers398122809
pharmgkbrs398122809
gwascentralrs398122809
openSNPrs398122809
23andMers398122809
23andMe allrs398122809
SNP Nexus

SNPshotrs398122809
SNPdbers398122809
MSV3drs398122809
GWAS Ctlgrs398122809
Max Magnitude0
ClinVar
Risk rs398122809(AGA;AGA)
Alt rs398122809(AGA;AGA)
Reference rs398122809(;)
Significance Pathogenic
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.534213_534215dupTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022798.24,