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rs121913375

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913375(C;T)
Make rs121913375(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position140753339
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913375
ebirs121913375
HLIrs121913375
Exacrs121913375
Varsomers121913375
Maprs121913375
PheGenIrs121913375
hapmaprs121913375
1000 genomesrs121913375
hgdprs121913375
ensemblrs121913375
gopubmedrs121913375
geneviewrs121913375
scholarrs121913375
googlers121913375
pharmgkbrs121913375
gwascentralrs121913375
openSNPrs121913375
23andMers121913375
23andMe allrs121913375
SNP Nexus

SNPshotrs121913375
SNPdbers121913375
MSV3drs121913375
GWAS Ctlgrs121913375
Max Magnitude0
ClinVar
Risk rs121913375(T;T)
Alt rs121913375(T;T)
Reference rs121913375(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140453139G>A
CLNSRC ClinVar
CLNACC RCV000033334.4,