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rs121913337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913337(A;A)
Make rs121913337(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753353
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913337
dbSNP (old)rs121913337
ClinGenrs121913337
ebirs121913337
HLIrs121913337
Exacrs121913337
Gnomadrs121913337
Varsomers121913337
Maprs121913337
PheGenIrs121913337
Biobankrs121913337
1000 genomesrs121913337
hgdprs121913337
ensemblrs121913337
gopubmedrs121913337
geneviewrs121913337
scholarrs121913337
googlers121913337
pharmgkbrs121913337
gwascentralrs121913337
openSNPrs121913337
23andMers121913337
23andMe allrs121913337
SNPshotrs121913337
SNPdbers121913337
MSV3drs121913337
GWAS Ctlgrs121913337
Max Magnitude0
ClinVar
Risk rs121913337(A;A) rs121913337(G;G)
Alt rs121913337(A;A) rs121913337(G;G)
Reference Rs121913337(T;T)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453153A>C; NC_000007.13:g.140453153A>T
CLNSRC
CLNACC RCV000428481.1, RCV000438728.1,