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rs111033726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033726(C;C)
Make rs111033726(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648349
GeneGALT
is asnp
is mentioned by
dbSNPrs111033726
ebirs111033726
HLIrs111033726
Exacrs111033726
Varsomers111033726
Maprs111033726
PheGenIrs111033726
hapmaprs111033726
1000 genomesrs111033726
hgdprs111033726
ensemblrs111033726
gopubmedrs111033726
geneviewrs111033726
scholarrs111033726
googlers111033726
pharmgkbrs111033726
gwascentralrs111033726
openSNPrs111033726
23andMers111033726
23andMe allrs111033726
SNP Nexus

SNPshotrs111033726
SNPdbers111033726
MSV3drs111033726
GWAS Ctlgrs111033726
Max Magnitude0
ClinVar
Risk rs111033726(C;C)
Alt rs111033726(C;C)
Reference rs111033726(T;T)
Significance Pathogenic
Disease Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Variation info
Gene GALT
CLNDBN Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Reversed 0
HGVS NC_000009.11:g.34648346T>C
CLNSRC ARUP GALT OMIM Allelic Variant
CLNACC RCV000003808.1,