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rs397516897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGA;TGA) 0 common in clinvar
Make rs397516897(-;-)
Make rs397516897(-;TGA)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753334
GeneBRAF
is asnp
is mentioned by
dbSNPrs397516897
ebirs397516897
HLIrs397516897
Exacrs397516897
Varsomers397516897
Maprs397516897
PheGenIrs397516897
hapmaprs397516897
1000 genomesrs397516897
hgdprs397516897
ensemblrs397516897
gopubmedrs397516897
geneviewrs397516897
scholarrs397516897
googlers397516897
pharmgkbrs397516897
gwascentralrs397516897
openSNPrs397516897
23andMers397516897
23andMe allrs397516897
SNP Nexus

SNPshotrs397516897
SNPdbers397516897
MSV3drs397516897
GWAS Ctlgrs397516897
Max Magnitude0
ClinVar
Risk rs397516897(;)
Alt rs397516897(;)
Reference rs397516897(TGA;TGA)
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.140453134_140453136delTCA
CLNSRC COSMIC
CLNACC RCV000037937.2,