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rs397514553

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514553(C;T)
Make rs397514553(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114716060
GeneNRAS
is asnp
is mentioned by
dbSNPrs397514553
ebirs397514553
HLIrs397514553
Exacrs397514553
Varsomers397514553
Maprs397514553
PheGenIrs397514553
hapmaprs397514553
1000 genomesrs397514553
hgdprs397514553
ensemblrs397514553
gopubmedrs397514553
geneviewrs397514553
scholarrs397514553
googlers397514553
pharmgkbrs397514553
gwascentralrs397514553
openSNPrs397514553
23andMers397514553
23andMe allrs397514553
SNP Nexus

SNPshotrs397514553
SNPdbers397514553
MSV3drs397514553
GWAS Ctlgrs397514553
Max Magnitude0
ClinVar
Risk rs397514553(T;T)
Alt rs397514553(T;T)
Reference rs397514553(C;C)
Significance Pathogenic
Disease Epidermal nevus Noonan syndrome 1
Variation info
Gene NRAS
CLNDBN Epidermal nevus Noonan syndrome 1
Reversed 1
HGVS NC_000001.10:g.115258681G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032848.4, RCV000208568.1,