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rs121917759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917759(C;T)
Make rs121917759(T;T)
ReferenceGRCh37.p5 37.3/135
Chromosome11
Position533466
GeneHRAS
is asnp
is mentioned by
dbSNPrs121917759
ebirs121917759
HLIrs121917759
Exacrs121917759
Varsomers121917759
Maprs121917759
PheGenIrs121917759
hapmaprs121917759
1000 genomesrs121917759
hgdprs121917759
ensemblrs121917759
gopubmedrs121917759
geneviewrs121917759
scholarrs121917759
googlers121917759
pharmgkbrs121917759
gwascentralrs121917759
openSNPrs121917759
23andMers121917759
23andMe allrs121917759
SNP Nexus

SNPshotrs121917759
SNPdbers121917759
MSV3drs121917759
GWAS Ctlgrs121917759
Max Magnitude0
OMIM190020
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121917759(T;T)
Alt rs121917759(T;T)
Reference rs121917759(C;C)
Significance Other
Disease Costello syndrome
Variation info
Gene HRAS
CLNDBN Costello syndrome
Reversed 1
HGVS NC_000011.9:g.533466G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013445.17,