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rs121913335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913335(A;C)
Make rs121913335(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753375
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913335
dbSNP (old)rs121913335
ClinGenrs121913335
ebirs121913335
HLIrs121913335
Exacrs121913335
Gnomadrs121913335
Varsomers121913335
Maprs121913335
PheGenIrs121913335
Biobankrs121913335
1000 genomesrs121913335
hgdprs121913335
ensemblrs121913335
gopubmedrs121913335
geneviewrs121913335
scholarrs121913335
googlers121913335
pharmgkbrs121913335
gwascentralrs121913335
openSNPrs121913335
23andMers121913335
23andMe allrs121913335
SNPshotrs121913335
SNPdbers121913335
MSV3drs121913335
GWAS Ctlgrs121913335
Max Magnitude0
ClinVar
Risk rs121913335(C;C)
Alt rs121913335(C;C)
Reference Rs121913335(A;A)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene BRAF
CLNDBN Neoplasm
Reversed 1
HGVS NC_000007.13:g.140453175T>G
CLNSRC
CLNACC RCV000434950.1,