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rs397507470

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507470(A;A)
Make rs397507470(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801488
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507470
ebirs397507470
HLIrs397507470
Exacrs397507470
Varsomers397507470
Maprs397507470
PheGenIrs397507470
hapmaprs397507470
1000 genomesrs397507470
hgdprs397507470
ensemblrs397507470
gopubmedrs397507470
geneviewrs397507470
scholarrs397507470
googlers397507470
pharmgkbrs397507470
gwascentralrs397507470
openSNPrs397507470
23andMers397507470
23andMe allrs397507470
SNP Nexus

SNPshotrs397507470
SNPdbers397507470
MSV3drs397507470
GWAS Ctlgrs397507470
Max Magnitude0
ClinVar
Risk rs397507470(A;A)
Alt rs397507470(A;A)
Reference rs397507470(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140501288G>T
CLNSRC ClinVar
CLNACC RCV000033290.4,