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rs121913363

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913363(A;G)
Make rs121913363(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753361
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913363
dbSNP (old)rs121913363
ClinGenrs121913363
ebirs121913363
HLIrs121913363
Exacrs121913363
Gnomadrs121913363
Varsomers121913363
Maprs121913363
PheGenIrs121913363
Biobankrs121913363
1000 genomesrs121913363
hgdprs121913363
ensemblrs121913363
gopubmedrs121913363
geneviewrs121913363
scholarrs121913363
googlers121913363
pharmgkbrs121913363
gwascentralrs121913363
openSNPrs121913363
23andMers121913363
23andMe allrs121913363
SNPshotrs121913363
SNPdbers121913363
MSV3drs121913363
GWAS Ctlgrs121913363
Max Magnitude0
ClinVar
Risk rs121913363(G;G)
Alt rs121913363(G;G)
Reference Rs121913363(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453161T>C
CLNSRC
CLNACC RCV000427646.1,