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rs121913351

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913351(C;C)
Make rs121913351(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140781611
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913351
ebirs121913351
HLIrs121913351
Exacrs121913351
Varsomers121913351
Maprs121913351
PheGenIrs121913351
hapmaprs121913351
1000 genomesrs121913351
hgdprs121913351
ensemblrs121913351
gopubmedrs121913351
geneviewrs121913351
scholarrs121913351
googlers121913351
pharmgkbrs121913351
gwascentralrs121913351
openSNPrs121913351
23andMers121913351
23andMe allrs121913351
SNP Nexus

SNPshotrs121913351
SNPdbers121913351
MSV3drs121913351
GWAS Ctlgrs121913351
Max Magnitude0
OMIM164757
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913351(A,C,T;A,C,T)
Alt rs121913351(A,C,T;A,C,T)
Reference rs121913351(G;G)
Significance Pathogenic
Disease Adenocarcinoma of lung Non-small cell lung cancer
Variation info
Gene BRAF
CLNDBN Adenocarcinoma of lung Non-small cell lung cancer
Reversed 1
HGVS NC_000007.13:g.140481411C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015001.5, RCV000037916.2,