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rs397507467

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507467(C;C)
Make rs397507467(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801532
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507467
ebirs397507467
HLIrs397507467
Exacrs397507467
Varsomers397507467
Maprs397507467
PheGenIrs397507467
hapmaprs397507467
1000 genomesrs397507467
hgdprs397507467
ensemblrs397507467
gopubmedrs397507467
geneviewrs397507467
scholarrs397507467
googlers397507467
pharmgkbrs397507467
gwascentralrs397507467
openSNPrs397507467
23andMers397507467
23andMe allrs397507467
SNP Nexus

SNPshotrs397507467
SNPdbers397507467
MSV3drs397507467
GWAS Ctlgrs397507467
Max Magnitude0
ClinVar
Risk rs397507467(C;C)
Alt rs397507467(C;C)
Reference rs397507467(T;T)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140501332A>G
CLNSRC ClinVar
CLNACC RCV000033286.2,