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rs111033675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033675(A;A)
Make rs111033675(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647696
GeneGALT
is asnp
is mentioned by
dbSNPrs111033675
ebirs111033675
HLIrs111033675
Exacrs111033675
Varsomers111033675
Maprs111033675
PheGenIrs111033675
hapmaprs111033675
1000 genomesrs111033675
hgdprs111033675
ensemblrs111033675
gopubmedrs111033675
geneviewrs111033675
scholarrs111033675
googlers111033675
pharmgkbrs111033675
gwascentralrs111033675
openSNPrs111033675
23andMers111033675
23andMe allrs111033675
SNP Nexus

SNPshotrs111033675
SNPdbers111033675
MSV3drs111033675
GWAS Ctlgrs111033675
Max Magnitude0
ClinVar
Risk rs111033675(A;A)
Alt rs111033675(A;A)
Reference rs111033675(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.34647693G>A
CLNSRC ARUP GALT
CLNACC RCV000022093.1,