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rs397516826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516826(C;C)
Make rs397516826(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12604202
GeneRAF1
is asnp
is mentioned by
dbSNPrs397516826
ebirs397516826
HLIrs397516826
Exacrs397516826
Varsomers397516826
Maprs397516826
PheGenIrs397516826
hapmaprs397516826
1000 genomesrs397516826
hgdprs397516826
ensemblrs397516826
gopubmedrs397516826
geneviewrs397516826
scholarrs397516826
googlers397516826
pharmgkbrs397516826
gwascentralrs397516826
openSNPrs397516826
23andMers397516826
23andMe allrs397516826
SNP Nexus

SNPshotrs397516826
SNPdbers397516826
MSV3drs397516826
GWAS Ctlgrs397516826
Max Magnitude0
ClinVar
Risk rs397516826(C,T;C,T)
Alt rs397516826(C,T;C,T)
Reference rs397516826(G;G)
Significance Pathogenic
Disease Noonan syndrome Rasopathy
Variation info
Gene RAF1
CLNDBN Noonan syndrome Rasopathy
Reversed 1
HGVS NC_000003.11:g.12645701C>A; NC_000003.11:g.12645701C>G
CLNSRC ClinVar
CLNACC RCV000037701.2, RCV000159072.1, RCV000037700.2,