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rs397507477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507477(C;T)
Make rs397507477(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140777995
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507477
ebirs397507477
HLIrs397507477
Exacrs397507477
Varsomers397507477
Maprs397507477
PheGenIrs397507477
hapmaprs397507477
1000 genomesrs397507477
hgdprs397507477
ensemblrs397507477
gopubmedrs397507477
geneviewrs397507477
scholarrs397507477
googlers397507477
pharmgkbrs397507477
gwascentralrs397507477
openSNPrs397507477
23andMers397507477
23andMe allrs397507477
SNP Nexus

SNPshotrs397507477
SNPdbers397507477
MSV3drs397507477
GWAS Ctlgrs397507477
Max Magnitude0
ClinVar
Risk rs397507477(T;T)
Alt rs397507477(T;T)
Reference rs397507477(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140477795G>A
CLNSRC ClinVar
CLNACC RCV000033319.5,