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rs397516896

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516896(A;A)
Make rs397516896(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753355
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516896
ebirs397516896
HLIrs397516896
Exacrs397516896
Varsomers397516896
Maprs397516896
PheGenIrs397516896
hapmaprs397516896
1000 genomesrs397516896
hgdprs397516896
ensemblrs397516896
gopubmedrs397516896
geneviewrs397516896
scholarrs397516896
googlers397516896
pharmgkbrs397516896
gwascentralrs397516896
openSNPrs397516896
23andMers397516896
23andMe allrs397516896
SNP Nexus

SNPshotrs397516896
SNPdbers397516896
MSV3drs397516896
GWAS Ctlgrs397516896
Max Magnitude0
ClinVar
Risk rs397516896(A;A)
Alt rs397516896(A;A)
Reference rs397516896(G;G)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene BRAF
CLNDBN Non-small cell lung cancer
Reversed 1
HGVS NC_000007.13:g.140453155C>T
CLNSRC COSMIC
CLNACC RCV000037931.2,