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rs74103423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74103423(A;A)
Make rs74103423(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position100216085
GeneDBT
is asnp
is mentioned by
dbSNPrs74103423
ebirs74103423
HLIrs74103423
Exacrs74103423
Varsomers74103423
Maprs74103423
PheGenIrs74103423
hapmaprs74103423
1000 genomesrs74103423
hgdprs74103423
ensemblrs74103423
gopubmedrs74103423
geneviewrs74103423
scholarrs74103423
googlers74103423
pharmgkbrs74103423
gwascentralrs74103423
openSNPrs74103423
23andMers74103423
23andMe allrs74103423
SNP Nexus

SNPshotrs74103423
SNPdbers74103423
MSV3drs74103423
GWAS Ctlgrs74103423
Max Magnitude0
ClinVar
Risk rs74103423(A;A)
Alt rs74103423(A;A)
Reference rs74103423(C;C)
Significance Pathogenic
Disease not provided Maple syrup urine disease
Variation info
Gene DBT
CLNDBN not provided Maple syrup urine disease
Reversed 0
HGVS NC_000001.10:g.100681641C>A
CLNSRC HGMD
CLNACC RCV000079951.3, RCV000179397.1,