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rs121913378

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913378(G;T)
Make rs121913378(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753337
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913378
ebirs121913378
HLIrs121913378
Exacrs121913378
Varsomers121913378
Maprs121913378
PheGenIrs121913378
hapmaprs121913378
1000 genomesrs121913378
hgdprs121913378
ensemblrs121913378
gopubmedrs121913378
geneviewrs121913378
scholarrs121913378
googlers121913378
pharmgkbrs121913378
gwascentralrs121913378
openSNPrs121913378
23andMers121913378
23andMe allrs121913378
SNP Nexus

SNPshotrs121913378
SNPdbers121913378
MSV3drs121913378
GWAS Ctlgrs121913378
Max Magnitude0
ClinVar
Risk rs121913378(A,T;A,T)
Alt rs121913378(A,T;A,T)
Reference rs121913378(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.140453137C>A; NC_000007.13:g.140453137C>T
CLNSRC ClinVar
CLNACC RCV000037935.2, RCV000037934.2,