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rs121913361

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913361(C;C)
Make rs121913361(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753349
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913361
ebirs121913361
HLIrs121913361
Exacrs121913361
Varsomers121913361
Maprs121913361
PheGenIrs121913361
hapmaprs121913361
1000 genomesrs121913361
hgdprs121913361
ensemblrs121913361
gopubmedrs121913361
geneviewrs121913361
scholarrs121913361
googlers121913361
pharmgkbrs121913361
gwascentralrs121913361
openSNPrs121913361
23andMers121913361
23andMe allrs121913361
SNP Nexus

SNPshotrs121913361
SNPdbers121913361
MSV3drs121913361
GWAS Ctlgrs121913361
Max Magnitude0
ClinVar
Risk rs121913361(C,T;C,T)
Alt rs121913361(C,T;C,T)
Reference rs121913361(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRAF
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.140453149C>A
CLNSRC ClinVar
CLNACC RCV000037933.4,