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rs121913371

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913371(C;T)
Make rs121913371(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140781678
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913371
dbSNP (old)rs121913371
ClinGenrs121913371
ebirs121913371
HLIrs121913371
Exacrs121913371
Gnomadrs121913371
Varsomers121913371
LitVarrs121913371
Maprs121913371
PheGenIrs121913371
Biobankrs121913371
1000 genomesrs121913371
hgdprs121913371
ensemblrs121913371
gopubmedrs121913371
geneviewrs121913371
scholarrs121913371
googlers121913371
pharmgkbrs121913371
gwascentralrs121913371
openSNPrs121913371
23andMers121913371
23andMe allrs121913371
SNPshotrs121913371
SNPdbers121913371
MSV3drs121913371
GWAS Ctlgrs121913371
Max Magnitude0
ClinVar
Risk rs121913371(A;A) rs121913371(T;T)
Alt rs121913371(A;A) rs121913371(T;T)
Reference Rs121913371(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140481478G>A
CLNSRC
CLNACC RCV000435724.1,