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rs111033766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033766(C;G)
Make rs111033766(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648888
GeneGALT
is asnp
is mentioned by
dbSNPrs111033766
ebirs111033766
HLIrs111033766
Exacrs111033766
Varsomers111033766
Maprs111033766
PheGenIrs111033766
hapmaprs111033766
1000 genomesrs111033766
hgdprs111033766
ensemblrs111033766
gopubmedrs111033766
geneviewrs111033766
scholarrs111033766
googlers111033766
pharmgkbrs111033766
gwascentralrs111033766
openSNPrs111033766
23andMers111033766
23andMe allrs111033766
SNP Nexus

SNPshotrs111033766
SNPdbers111033766
MSV3drs111033766
GWAS Ctlgrs111033766
Max Magnitude0
ClinVar
Risk rs111033766(G,T;G,T)
Alt rs111033766(G,T;G,T)
Reference rs111033766(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.34648885C>G
CLNSRC ARUP GALT
CLNACC RCV000022209.1,