Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913353

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913353(C;C)
Make rs121913353(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140781612
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913353
ebirs121913353
HLIrs121913353
Exacrs121913353
Varsomers121913353
Maprs121913353
PheGenIrs121913353
hapmaprs121913353
1000 genomesrs121913353
hgdprs121913353
ensemblrs121913353
gopubmedrs121913353
geneviewrs121913353
scholarrs121913353
googlers121913353
pharmgkbrs121913353
gwascentralrs121913353
openSNPrs121913353
23andMers121913353
23andMe allrs121913353
SNP Nexus

SNPshotrs121913353
SNPdbers121913353
MSV3drs121913353
GWAS Ctlgrs121913353
Max Magnitude0
ClinVar
Risk rs121913353(A,C;A,C)
Alt rs121913353(A,C;A,C)
Reference rs121913353(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.140481412C>T
CLNSRC
CLNACC RCV000037915.2,