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rs111033644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033644(A;A)
Make rs111033644(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647101
GeneGALT
is asnp
is mentioned by
dbSNPrs111033644
ebirs111033644
HLIrs111033644
Exacrs111033644
Varsomers111033644
Maprs111033644
PheGenIrs111033644
hapmaprs111033644
1000 genomesrs111033644
hgdprs111033644
ensemblrs111033644
gopubmedrs111033644
geneviewrs111033644
scholarrs111033644
googlers111033644
pharmgkbrs111033644
gwascentralrs111033644
openSNPrs111033644
23andMers111033644
23andMe allrs111033644
SNP Nexus

SNPshotrs111033644
SNPdbers111033644
MSV3drs111033644
GWAS Ctlgrs111033644
Max Magnitude0
ClinVar
Risk rs111033644(A;A)
Alt rs111033644(A;A)
Reference rs111033644(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.34647098T>A
CLNSRC ARUP GALT
CLNACC RCV000022050.1,