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rs121913362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913362(A;G)
Make rs121913362(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753359
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913362
dbSNP (old)rs121913362
ClinGenrs121913362
ebirs121913362
HLIrs121913362
Exacrs121913362
Gnomadrs121913362
Varsomers121913362
Maprs121913362
PheGenIrs121913362
Biobankrs121913362
1000 genomesrs121913362
hgdprs121913362
ensemblrs121913362
gopubmedrs121913362
geneviewrs121913362
scholarrs121913362
googlers121913362
pharmgkbrs121913362
gwascentralrs121913362
openSNPrs121913362
23andMers121913362
23andMe allrs121913362
SNPshotrs121913362
SNPdbers121913362
MSV3drs121913362
GWAS Ctlgrs121913362
Max Magnitude0
ClinVar
Risk rs121913362(G;G)
Alt rs121913362(G;G)
Reference Rs121913362(A;A)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene BRAF
CLNDBN Neoplasm
Reversed 1
HGVS NC_000007.13:g.140453159T>C
CLNSRC
CLNACC RCV000437742.1,