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rs397507480

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507480(G;G)
Make rs397507480(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140754233
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507480
ebirs397507480
HLIrs397507480
Exacrs397507480
Varsomers397507480
Maprs397507480
PheGenIrs397507480
hapmaprs397507480
1000 genomesrs397507480
hgdprs397507480
ensemblrs397507480
gopubmedrs397507480
geneviewrs397507480
scholarrs397507480
googlers397507480
pharmgkbrs397507480
gwascentralrs397507480
openSNPrs397507480
23andMers397507480
23andMe allrs397507480
SNP Nexus

SNPshotrs397507480
SNPdbers397507480
MSV3drs397507480
GWAS Ctlgrs397507480
Max Magnitude0
ClinVar
Risk rs397507480(G;G)
Alt rs397507480(G;G)
Reference rs397507480(T;T)
Significance Pathogenic
Disease Rasopathy Cardiofaciocutaneous syndrome not provided
Variation info
Gene BRAF
CLNDBN Rasopathy Cardiofaciocutaneous syndrome not provided
Reversed 1
HGVS NC_000007.13:g.140454033A>C
CLNSRC ClinVar
CLNACC RCV000033327.2, RCV000037927.2, RCV000207514.1,