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rs185492864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs185492864(A;A)
Make rs185492864(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position100214855
GeneDBT
is asnp
is mentioned by
dbSNPrs185492864
ebirs185492864
HLIrs185492864
Exacrs185492864
Varsomers185492864
Maprs185492864
PheGenIrs185492864
hapmaprs185492864
1000 genomesrs185492864
hgdprs185492864
ensemblrs185492864
gopubmedrs185492864
geneviewrs185492864
scholarrs185492864
googlers185492864
pharmgkbrs185492864
gwascentralrs185492864
openSNPrs185492864
23andMers185492864
23andMe allrs185492864
SNP Nexus

SNPshotrs185492864
SNPdbers185492864
MSV3drs185492864
GWAS Ctlgrs185492864
Max Magnitude0
ClinVar
Risk rs185492864(A;A)
Alt rs185492864(A;A)
Reference rs185492864(G;G)
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.100680411G>A
CLNSRC HGMD
CLNACC RCV000079959.5, RCV000179836.1,