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rs398123668

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123668(-;-)
Make rs398123668(-;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position100230806
GeneDBT
is asnp
is mentioned by
dbSNPrs398123668
ebirs398123668
HLIrs398123668
Exacrs398123668
Varsomers398123668
Maprs398123668
PheGenIrs398123668
hapmaprs398123668
1000 genomesrs398123668
hgdprs398123668
ensemblrs398123668
gopubmedrs398123668
geneviewrs398123668
scholarrs398123668
googlers398123668
pharmgkbrs398123668
gwascentralrs398123668
openSNPrs398123668
23andMers398123668
23andMe allrs398123668
SNP Nexus

SNPshotrs398123668
SNPdbers398123668
MSV3drs398123668
GWAS Ctlgrs398123668
Max Magnitude0
ClinVar
Risk rs398123668(;)
Alt rs398123668(;)
Reference rs398123668(A;A)
Significance Pathogenic
Disease not provided Maple syrup urine disease
Variation info
Gene DBT
CLNDBN not provided Maple syrup urine disease
Reversed 1
HGVS NC_000001.10:g.100696362delT
CLNSRC ClinVar
CLNACC RCV000079944.3, RCV000178171.1,