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rs397516892

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516892(A;A)
Make rs397516892(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position140778066
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516892
ebirs397516892
HLIrs397516892
Exacrs397516892
Varsomers397516892
Maprs397516892
PheGenIrs397516892
hapmaprs397516892
1000 genomesrs397516892
hgdprs397516892
ensemblrs397516892
gopubmedrs397516892
geneviewrs397516892
scholarrs397516892
googlers397516892
pharmgkbrs397516892
gwascentralrs397516892
openSNPrs397516892
23andMers397516892
23andMe allrs397516892
SNP Nexus

SNPshotrs397516892
SNPdbers397516892
MSV3drs397516892
GWAS Ctlgrs397516892
Max Magnitude0
ClinVar
Risk rs397516892(A;A)
Alt rs397516892(A;A)
Reference rs397516892(C;C)
Significance Probable-Pathogenic
Disease Cardiofaciocutaneous syndrome
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140477866G>T
CLNSRC ClinVar
CLNACC RCV000037921.2,