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rs121913372

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs121913372(AG;TT)
Make rs121913372(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140753321
GeneBRAF
is asnp
is mentioned by
dbSNPrs121913372
dbSNP (old)rs121913372
ClinGenrs121913372
ebirs121913372
HLIrs121913372
Exacrs121913372
Gnomadrs121913372
Varsomers121913372
Maprs121913372
PheGenIrs121913372
Biobankrs121913372
1000 genomesrs121913372
hgdprs121913372
ensemblrs121913372
gopubmedrs121913372
geneviewrs121913372
scholarrs121913372
googlers121913372
pharmgkbrs121913372
gwascentralrs121913372
openSNPrs121913372
23andMers121913372
23andMe allrs121913372
SNPshotrs121913372
SNPdbers121913372
MSV3drs121913372
GWAS Ctlgrs121913372
Max Magnitude0
ClinVar
Risk rs121913372(TT;TT)
Alt rs121913372(TT;TT)
Reference Rs121913372(AG;AG)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene BRAF
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000007.13:g.140453121_140453122delCTinsAA
CLNSRC
CLNACC RCV000419349.1,