Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913349

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913349(C;C)
Make rs121913349(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position140781618
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913349
dbSNP (old)rs121913349
ClinGenrs121913349
ebirs121913349
HLIrs121913349
Exacrs121913349
Gnomadrs121913349
Varsomers121913349
Maprs121913349
PheGenIrs121913349
Biobankrs121913349
1000 genomesrs121913349
hgdprs121913349
ensemblrs121913349
gopubmedrs121913349
geneviewrs121913349
scholarrs121913349
googlers121913349
pharmgkbrs121913349
gwascentralrs121913349
openSNPrs121913349
23andMers121913349
23andMe allrs121913349
SNPshotrs121913349
SNPdbers121913349
MSV3drs121913349
GWAS Ctlgrs121913349
Max Magnitude0
ClinVar
Risk rs121913349(A;A) rs121913349(C;C)
Alt rs121913349(A;A) rs121913349(C;C)
Reference Rs121913349(G;G)
Significance Pathogenic
Disease not provided Malignant melanoma
Variation info
Gene BRAF
CLNDBN not provided Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140481418C>G; NC_000007.13:g.140481418C>T
CLNSRC
CLNACC RCV000304268.1, RCV000413557.1, RCV000429423.1,