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rs121913373

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913373(A;A)
Make rs121913373(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753321
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913373
dbSNP (old)rs121913373
ClinGenrs121913373
ebirs121913373
HLIrs121913373
Exacrs121913373
Gnomadrs121913373
Varsomers121913373
Maprs121913373
PheGenIrs121913373
Biobankrs121913373
1000 genomesrs121913373
hgdprs121913373
ensemblrs121913373
gopubmedrs121913373
geneviewrs121913373
scholarrs121913373
googlers121913373
pharmgkbrs121913373
gwascentralrs121913373
openSNPrs121913373
23andMers121913373
23andMe allrs121913373
SNPshotrs121913373
SNPdbers121913373
MSV3drs121913373
GWAS Ctlgrs121913373
Max Magnitude0
ClinVar
Risk rs121913373(A;A)
Alt rs121913373(A;A)
Reference Rs121913373(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453121C>T
CLNSRC
CLNACC RCV000437021.1,