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rs111033767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033767(A;G)
Make rs111033767(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648996
GeneGALT
is asnp
is mentioned by
dbSNPrs111033767
ebirs111033767
HLIrs111033767
Exacrs111033767
Varsomers111033767
Maprs111033767
PheGenIrs111033767
hapmaprs111033767
1000 genomesrs111033767
hgdprs111033767
ensemblrs111033767
gopubmedrs111033767
geneviewrs111033767
scholarrs111033767
googlers111033767
pharmgkbrs111033767
gwascentralrs111033767
openSNPrs111033767
23andMers111033767
23andMe allrs111033767
SNP Nexus

SNPshotrs111033767
SNPdbers111033767
MSV3drs111033767
GWAS Ctlgrs111033767
Max Magnitude0
ClinVar
Risk rs111033767(G;G)
Alt rs111033767(G;G)
Reference rs111033767(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.34648993A>G
CLNSRC ARUP GALT
CLNACC RCV000022214.1,