Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033747(A;A)
Make rs111033747(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648427
GeneGALT
is asnp
is mentioned by
dbSNPrs111033747
ebirs111033747
HLIrs111033747
Exacrs111033747
Varsomers111033747
Maprs111033747
PheGenIrs111033747
hapmaprs111033747
1000 genomesrs111033747
hgdprs111033747
ensemblrs111033747
gopubmedrs111033747
geneviewrs111033747
scholarrs111033747
googlers111033747
pharmgkbrs111033747
gwascentralrs111033747
openSNPrs111033747
23andMers111033747
23andMe allrs111033747
SNP Nexus

SNPshotrs111033747
SNPdbers111033747
MSV3drs111033747
GWAS Ctlgrs111033747
Max Magnitude0
ClinVar
Risk rs111033747(A;A)
Alt rs111033747(A;A)
Reference rs111033747(G;G)
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.34648424G>A
CLNSRC ARUP GALT
CLNACC RCV000022176.1,