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rs397507481

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507481(C;G)
Make rs397507481(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140754206
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507481
ebirs397507481
HLIrs397507481
Exacrs397507481
Varsomers397507481
Maprs397507481
PheGenIrs397507481
hapmaprs397507481
1000 genomesrs397507481
hgdprs397507481
ensemblrs397507481
gopubmedrs397507481
geneviewrs397507481
scholarrs397507481
googlers397507481
pharmgkbrs397507481
gwascentralrs397507481
openSNPrs397507481
23andMers397507481
23andMe allrs397507481
SNP Nexus

SNPshotrs397507481
SNPdbers397507481
MSV3drs397507481
GWAS Ctlgrs397507481
Max Magnitude0
ClinVar
Risk rs397507481(A,G;A,G)
Alt rs397507481(A,G;A,G)
Reference rs397507481(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140454006G>C; NC_000007.13:g.140454006G>T
CLNSRC ClinVar
CLNACC RCV000033328.3, RCV000157823.1,