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rs121913340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913340(A;A)
Make rs121913340(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753379
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913340
dbSNP (old)rs121913340
ClinGenrs121913340
ebirs121913340
HLIrs121913340
Exacrs121913340
Gnomadrs121913340
Varsomers121913340
LitVarrs121913340
Maprs121913340
PheGenIrs121913340
Biobankrs121913340
1000 genomesrs121913340
hgdprs121913340
ensemblrs121913340
gopubmedrs121913340
geneviewrs121913340
scholarrs121913340
googlers121913340
pharmgkbrs121913340
gwascentralrs121913340
openSNPrs121913340
23andMers121913340
23andMe allrs121913340
SNPshotrs121913340
SNPdbers121913340
MSV3drs121913340
GWAS Ctlgrs121913340
Max Magnitude0
ClinVar
Risk rs121913340(A;A)
Alt rs121913340(A;A)
Reference Rs121913340(G;G)
Significance Probable-Pathogenic
Disease not specified Malignant melanoma Neoplasm
Variation info
Gene BRAF
CLNDBN not specified Malignant melanoma Neoplasm
Reversed 1
HGVS NC_000007.13:g.140453179C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000037930.2, RCV000419782.1, RCV000437874.1,