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rs111033764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033764(C;G)
Make rs111033764(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648867
GeneGALT
is asnp
is mentioned by
dbSNPrs111033764
ebirs111033764
HLIrs111033764
Exacrs111033764
Varsomers111033764
Maprs111033764
PheGenIrs111033764
hapmaprs111033764
1000 genomesrs111033764
hgdprs111033764
ensemblrs111033764
gopubmedrs111033764
geneviewrs111033764
scholarrs111033764
googlers111033764
pharmgkbrs111033764
gwascentralrs111033764
openSNPrs111033764
23andMers111033764
23andMe allrs111033764
SNP Nexus

SNPshotrs111033764
SNPdbers111033764
MSV3drs111033764
GWAS Ctlgrs111033764
Max Magnitude0
ClinVar
Risk rs111033764(G;G)
Alt rs111033764(G;G)
Reference rs111033764(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.34648864C>G
CLNSRC ARUP GALT
CLNACC RCV000022206.1,