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rs397507476

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507476(A;C)
Make rs397507476(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position140778011
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507476
ebirs397507476
HLIrs397507476
Exacrs397507476
Varsomers397507476
Maprs397507476
PheGenIrs397507476
hapmaprs397507476
1000 genomesrs397507476
hgdprs397507476
ensemblrs397507476
gopubmedrs397507476
geneviewrs397507476
scholarrs397507476
googlers397507476
pharmgkbrs397507476
gwascentralrs397507476
openSNPrs397507476
23andMers397507476
23andMe allrs397507476
SNP Nexus

SNPshotrs397507476
SNPdbers397507476
MSV3drs397507476
GWAS Ctlgrs397507476
Max Magnitude0
ClinVar
Risk rs397507476(C,T;C,T)
Alt rs397507476(C,T;C,T)
Reference rs397507476(A;A)
Significance Other
Disease Rasopathy not provided
Variation info
Gene BRAF
CLNDBN Rasopathy not provided
Reversed 1
HGVS NC_000007.13:g.140477811T>A; NC_000007.13:g.140477811T>G
CLNSRC ClinVar
CLNACC RCV000033314.2, RCV000207509.2,