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rs121913225

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913225(C;C)
Make rs121913225(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753351
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913225
dbSNP (old)rs121913225
ClinGenrs121913225
ebirs121913225
HLIrs121913225
Exacrs121913225
Gnomadrs121913225
Varsomers121913225
Maprs121913225
PheGenIrs121913225
Biobankrs121913225
1000 genomesrs121913225
hgdprs121913225
ensemblrs121913225
gopubmedrs121913225
geneviewrs121913225
scholarrs121913225
googlers121913225
pharmgkbrs121913225
gwascentralrs121913225
openSNPrs121913225
23andMers121913225
23andMe allrs121913225
SNPshotrs121913225
SNPdbers121913225
MSV3drs121913225
GWAS Ctlgrs121913225
Max Magnitude0
ClinVar
Risk rs121913225(C;C)
Alt rs121913225(C;C)
Reference Rs121913225(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453151A>G
CLNSRC
CLNACC RCV000444314.1,