Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507469

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507469(A;A)
Make rs397507469(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801503
GeneBRAF
is asnp
is mentioned by
dbSNPrs397507469
ebirs397507469
HLIrs397507469
Exacrs397507469
Varsomers397507469
Maprs397507469
PheGenIrs397507469
hapmaprs397507469
1000 genomesrs397507469
hgdprs397507469
ensemblrs397507469
gopubmedrs397507469
geneviewrs397507469
scholarrs397507469
googlers397507469
pharmgkbrs397507469
gwascentralrs397507469
openSNPrs397507469
23andMers397507469
23andMe allrs397507469
SNP Nexus

SNPshotrs397507469
SNPdbers397507469
MSV3drs397507469
GWAS Ctlgrs397507469
Max Magnitude0
ClinVar
Risk rs397507469(A;A)
Alt rs397507469(A;A)
Reference rs397507469(C;C)
Significance Pathogenic
Disease Rasopathy not provided
Variation info
Gene BRAF
CLNDBN Rasopathy not provided
Reversed 1
HGVS NC_000007.13:g.140501303G>T
CLNSRC ClinVar
CLNACC RCV000033288.5, RCV000212151.1,