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rs121917758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917758(C;T)
Make rs121917758(T;T)
ReferenceGRCh37.p5 37.3/135
Chromosome11
Position533883
GeneHRAS
is asnp
is mentioned by
dbSNPrs121917758
ebirs121917758
HLIrs121917758
Exacrs121917758
Varsomers121917758
Maprs121917758
PheGenIrs121917758
hapmaprs121917758
1000 genomesrs121917758
hgdprs121917758
ensemblrs121917758
gopubmedrs121917758
geneviewrs121917758
scholarrs121917758
googlers121917758
pharmgkbrs121917758
gwascentralrs121917758
openSNPrs121917758
23andMers121917758
23andMe allrs121917758
SNP Nexus

SNPshotrs121917758
SNPdbers121917758
MSV3drs121917758
GWAS Ctlgrs121917758
Max Magnitude0
OMIM190020
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121917758(T;T)
Alt rs121917758(T;T)
Reference rs121917758(C;C)
Significance Pathogenic
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.533883G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013444.18,