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rs111033709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033709(A;A)
Make rs111033709(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647959
GeneGALT
is asnp
is mentioned by
dbSNPrs111033709
ebirs111033709
HLIrs111033709
Exacrs111033709
Varsomers111033709
Maprs111033709
PheGenIrs111033709
hapmaprs111033709
1000 genomesrs111033709
hgdprs111033709
ensemblrs111033709
gopubmedrs111033709
geneviewrs111033709
scholarrs111033709
googlers111033709
pharmgkbrs111033709
gwascentralrs111033709
openSNPrs111033709
23andMers111033709
23andMe allrs111033709
SNP Nexus

SNPshotrs111033709
SNPdbers111033709
MSV3drs111033709
GWAS Ctlgrs111033709
Max Magnitude0
ClinVar
Risk rs111033709(A;A)
Alt rs111033709(A;A)
Reference rs111033709(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.34647956C>A
CLNSRC ARUP GALT
CLNACC RCV000022126.1,