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rs121913376

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913376(G;T)
Make rs121913376(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140781597
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913376
ebirs121913376
HLIrs121913376
Exacrs121913376
Varsomers121913376
Maprs121913376
PheGenIrs121913376
hapmaprs121913376
1000 genomesrs121913376
hgdprs121913376
ensemblrs121913376
gopubmedrs121913376
geneviewrs121913376
scholarrs121913376
googlers121913376
pharmgkbrs121913376
gwascentralrs121913376
openSNPrs121913376
23andMers121913376
23andMe allrs121913376
SNP Nexus

SNPshotrs121913376
SNPdbers121913376
MSV3drs121913376
GWAS Ctlgrs121913376
Max Magnitude0
ClinVar
Risk rs121913376(A,T;A,T)
Alt rs121913376(A,T;A,T)
Reference rs121913376(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140481397C>A; NC_000007.13:g.140481397C>T
CLNSRC ClinVar
CLNACC RCV000033308.5, RCV000033309.4,