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rs111033731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033731(A;G)
Make rs111033731(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648332
GeneGALT
is asnp
is mentioned by
dbSNPrs111033731
ebirs111033731
HLIrs111033731
Exacrs111033731
Varsomers111033731
Maprs111033731
PheGenIrs111033731
hapmaprs111033731
1000 genomesrs111033731
hgdprs111033731
ensemblrs111033731
gopubmedrs111033731
geneviewrs111033731
scholarrs111033731
googlers111033731
pharmgkbrs111033731
gwascentralrs111033731
openSNPrs111033731
23andMers111033731
23andMe allrs111033731
SNP Nexus

SNPshotrs111033731
SNPdbers111033731
MSV3drs111033731
GWAS Ctlgrs111033731
Max Magnitude0
ClinVar
Risk rs111033731(G;G)
Alt rs111033731(G;G)
Reference rs111033731(A;A)
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.34648329A>G
CLNSRC ARUP GALT
CLNACC RCV000022154.1,