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rs397516895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516895(A;A)
Make rs397516895(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753392
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516895
ebirs397516895
HLIrs397516895
Exacrs397516895
Varsomers397516895
Maprs397516895
PheGenIrs397516895
hapmaprs397516895
1000 genomesrs397516895
hgdprs397516895
ensemblrs397516895
gopubmedrs397516895
geneviewrs397516895
scholarrs397516895
googlers397516895
pharmgkbrs397516895
gwascentralrs397516895
openSNPrs397516895
23andMers397516895
23andMe allrs397516895
SNP Nexus

SNPshotrs397516895
SNPdbers397516895
MSV3drs397516895
GWAS Ctlgrs397516895
Max Magnitude0
ClinVar
Risk rs397516895(A;A)
Alt rs397516895(A;A)
Reference rs397516895(T;T)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140453192A>T
CLNSRC ClinVar
CLNACC RCV000037929.2,