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rs397507473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507473(C;C)
Make rs397507473(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140781605
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507473
ebirs397507473
HLIrs397507473
Exacrs397507473
Varsomers397507473
Maprs397507473
PheGenIrs397507473
hapmaprs397507473
1000 genomesrs397507473
hgdprs397507473
ensemblrs397507473
gopubmedrs397507473
geneviewrs397507473
scholarrs397507473
googlers397507473
pharmgkbrs397507473
gwascentralrs397507473
openSNPrs397507473
23andMers397507473
23andMe allrs397507473
SNP Nexus

SNPshotrs397507473
SNPdbers397507473
MSV3drs397507473
GWAS Ctlgrs397507473
Max Magnitude0
ClinVar
Risk rs397507473(C;C)
Alt rs397507473(C;C)
Reference rs397507473(T;T)
Significance Pathogenic
Disease not provided Cardiofaciocutaneous syndrome
Variation info
Gene BRAF
CLNDBN not provided Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140481405A>G
CLNSRC ClinVar
CLNACC RCV000033305.5, RCV000037917.2,