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rs397507487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507487(C;T)
Make rs397507487(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140734743
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507487
ebirs397507487
HLIrs397507487
Exacrs397507487
Varsomers397507487
Maprs397507487
PheGenIrs397507487
hapmaprs397507487
1000 genomesrs397507487
hgdprs397507487
ensemblrs397507487
gopubmedrs397507487
geneviewrs397507487
scholarrs397507487
googlers397507487
pharmgkbrs397507487
gwascentralrs397507487
openSNPrs397507487
23andMers397507487
23andMe allrs397507487
SNP Nexus

SNPshotrs397507487
SNPdbers397507487
MSV3drs397507487
GWAS Ctlgrs397507487
Max Magnitude0
ClinVar
Risk rs397507487(T;T)
Alt rs397507487(T;T)
Reference rs397507487(C;C)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140434543G>A
CLNSRC ClinVar
CLNACC RCV000033345.2,