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rs398122808

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122808(-;-)
Make rs398122808(-;AGG)
Make rs398122808(AGG;AGG)
ReferenceGRCh37.p10 37.5/138
Chromosome11
Position534210
GeneHRAS
is asnp
is mentioned by
dbSNPrs398122808
ebirs398122808
HLIrs398122808
Exacrs398122808
Varsomers398122808
Maprs398122808
PheGenIrs398122808
hapmaprs398122808
1000 genomesrs398122808
hgdprs398122808
ensemblrs398122808
gopubmedrs398122808
geneviewrs398122808
scholarrs398122808
googlers398122808
pharmgkbrs398122808
gwascentralrs398122808
openSNPrs398122808
23andMers398122808
23andMe allrs398122808
SNP Nexus

SNPshotrs398122808
SNPdbers398122808
MSV3drs398122808
GWAS Ctlgrs398122808
Max Magnitude0
ClinVar
Risk rs398122808(AGG;AGG)
Alt rs398122808(AGG;AGG)
Reference rs398122808(;)
Significance Pathogenic
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.534211_534213dupCCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022797.22,