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rs111033826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033826(C;T)
Make rs111033826(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648160
GeneGALT
is asnp
is mentioned by
dbSNPrs111033826
ebirs111033826
HLIrs111033826
Exacrs111033826
Varsomers111033826
Maprs111033826
PheGenIrs111033826
hapmaprs111033826
1000 genomesrs111033826
hgdprs111033826
ensemblrs111033826
gopubmedrs111033826
geneviewrs111033826
scholarrs111033826
googlers111033826
pharmgkbrs111033826
gwascentralrs111033826
openSNPrs111033826
23andMers111033826
23andMe allrs111033826
SNP Nexus

SNPshotrs111033826
SNPdbers111033826
MSV3drs111033826
GWAS Ctlgrs111033826
Max Magnitude0
ClinVar
Risk rs111033826(T;T)
Alt rs111033826(T;T)
Reference rs111033826(C;C)
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.34648157C>T
CLNSRC ARUP GALT
CLNACC RCV000022147.1,