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rs111033761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033761(A;A)
Make rs111033761(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648851
GeneGALT
is asnp
is mentioned by
dbSNPrs111033761
ebirs111033761
HLIrs111033761
Exacrs111033761
Varsomers111033761
Maprs111033761
PheGenIrs111033761
hapmaprs111033761
1000 genomesrs111033761
hgdprs111033761
ensemblrs111033761
gopubmedrs111033761
geneviewrs111033761
scholarrs111033761
googlers111033761
pharmgkbrs111033761
gwascentralrs111033761
openSNPrs111033761
23andMers111033761
23andMe allrs111033761
SNP Nexus

SNPshotrs111033761
SNPdbers111033761
MSV3drs111033761
GWAS Ctlgrs111033761
Max Magnitude0
ClinVar
Risk rs111033761(A;A)
Alt rs111033761(A;A)
Reference rs111033761(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.34648848G>A
CLNSRC ARUP GALT
CLNACC RCV000022202.1,