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rs397509343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509343(G;G)
Make rs397509343(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801531
GeneBRAF
is asnp
is mentioned by
dbSNPrs397509343
ebirs397509343
HLIrs397509343
Exacrs397509343
Varsomers397509343
Maprs397509343
PheGenIrs397509343
hapmaprs397509343
1000 genomesrs397509343
hgdprs397509343
ensemblrs397509343
gopubmedrs397509343
geneviewrs397509343
scholarrs397509343
googlers397509343
pharmgkbrs397509343
gwascentralrs397509343
openSNPrs397509343
23andMers397509343
23andMe allrs397509343
SNP Nexus

SNPshotrs397509343
SNPdbers397509343
MSV3drs397509343
GWAS Ctlgrs397509343
Max Magnitude0
ClinVar
Risk rs397509343(G;G)
Alt rs397509343(G;G)
Reference rs397509343(T;T)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140501331A>C
CLNSRC ClinVar
CLNACC RCV000049222.1,