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rs121913366

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913366(A;A)
Make rs121913366(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753345
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913366
ebirs121913366
HLIrs121913366
Exacrs121913366
Varsomers121913366
Maprs121913366
PheGenIrs121913366
hapmaprs121913366
1000 genomesrs121913366
hgdprs121913366
ensemblrs121913366
gopubmedrs121913366
geneviewrs121913366
scholarrs121913366
googlers121913366
pharmgkbrs121913366
gwascentralrs121913366
openSNPrs121913366
23andMers121913366
23andMe allrs121913366
SNP Nexus

SNPshotrs121913366
SNPdbers121913366
MSV3drs121913366
GWAS Ctlgrs121913366
Max Magnitude0
OMIM164757
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913366(A,G;A,G)
Alt rs121913366(A,G;A,G)
Reference rs121913366(T;T)
Significance Pathogenic
Disease Adenocarcinoma of lung
Variation info
Gene BRAF
CLNDBN Adenocarcinoma of lung
Reversed 1
HGVS NC_000007.13:g.140453145A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015002.5,