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

rs397516893

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516893(G;G)
Make rs397516893(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140778048
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516893
ebirs397516893
HLIrs397516893
Exacrs397516893
Varsomers397516893
Maprs397516893
PheGenIrs397516893
hapmaprs397516893
1000 genomesrs397516893
hgdprs397516893
ensemblrs397516893
gopubmedrs397516893
geneviewrs397516893
scholarrs397516893
googlers397516893
pharmgkbrs397516893
gwascentralrs397516893
openSNPrs397516893
23andMers397516893
23andMe allrs397516893
SNP Nexus

SNPshotrs397516893
SNPdbers397516893
MSV3drs397516893
GWAS Ctlgrs397516893
Max Magnitude0
ClinVar
Risk rs397516893(G;G)
Alt rs397516893(G;G)
Reference rs397516893(T;T)
Significance Probable-Pathogenic
Disease Cardiofaciocutaneous syndrome
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000007.13:g.140477848A>C
CLNSRC ClinVar
CLNACC RCV000037922.2,