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rs111033828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033828(G;G)
Make rs111033828(G;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648148
GeneGALT
is asnp
is mentioned by
dbSNPrs111033828
ebirs111033828
HLIrs111033828
Exacrs111033828
Varsomers111033828
Maprs111033828
PheGenIrs111033828
hapmaprs111033828
1000 genomesrs111033828
hgdprs111033828
ensemblrs111033828
gopubmedrs111033828
geneviewrs111033828
scholarrs111033828
googlers111033828
pharmgkbrs111033828
gwascentralrs111033828
openSNPrs111033828
23andMers111033828
23andMe allrs111033828
SNP Nexus

SNPshotrs111033828
SNPdbers111033828
MSV3drs111033828
GWAS Ctlgrs111033828
Max Magnitude0
ClinVar
Risk rs111033828(G;G)
Alt rs111033828(G;G)
Reference rs111033828(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.34648145T>G
CLNSRC ARUP GALT
CLNACC RCV000022143.1,