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rs121913336

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913336(A;A)
Make rs121913336(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753374
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913336
dbSNP (old)rs121913336
ClinGenrs121913336
ebirs121913336
HLIrs121913336
Exacrs121913336
Gnomadrs121913336
Varsomers121913336
LitVarrs121913336
Maprs121913336
PheGenIrs121913336
Biobankrs121913336
1000 genomesrs121913336
hgdprs121913336
ensemblrs121913336
gopubmedrs121913336
geneviewrs121913336
scholarrs121913336
googlers121913336
pharmgkbrs121913336
gwascentralrs121913336
openSNPrs121913336
23andMers121913336
23andMe allrs121913336
SNPshotrs121913336
SNPdbers121913336
MSV3drs121913336
GWAS Ctlgrs121913336
Max Magnitude0
ClinVar
Risk rs121913336(A;A) rs121913336(G;G)
Alt rs121913336(A;A) rs121913336(G;G)
Reference Rs121913336(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene BRAF
CLNDBN Neoplasm
Reversed 1
HGVS NC_000007.13:g.140453174G>C; NC_000007.13:g.140453174G>T
CLNSRC
CLNACC RCV000420521.1, RCV000431213.1,