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rs397507486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507486(A;G)
Make rs397507486(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140739813
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507486
ebirs397507486
HLIrs397507486
Exacrs397507486
Varsomers397507486
Maprs397507486
PheGenIrs397507486
hapmaprs397507486
1000 genomesrs397507486
hgdprs397507486
ensemblrs397507486
gopubmedrs397507486
geneviewrs397507486
scholarrs397507486
googlers397507486
pharmgkbrs397507486
gwascentralrs397507486
openSNPrs397507486
23andMers397507486
23andMe allrs397507486
SNP Nexus

SNPshotrs397507486
SNPdbers397507486
MSV3drs397507486
GWAS Ctlgrs397507486
Max Magnitude0
ClinVar
Risk rs397507486(G;G)
Alt rs397507486(G;G)
Reference rs397507486(A;A)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140439613T>C
CLNSRC ClinVar
CLNACC RCV000033344.2,