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rs111033795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033795(A;A)
Make rs111033795(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649463
GeneGALT
is asnp
is mentioned by
dbSNPrs111033795
ebirs111033795
HLIrs111033795
Exacrs111033795
Varsomers111033795
Maprs111033795
PheGenIrs111033795
hapmaprs111033795
1000 genomesrs111033795
hgdprs111033795
ensemblrs111033795
gopubmedrs111033795
geneviewrs111033795
scholarrs111033795
googlers111033795
pharmgkbrs111033795
gwascentralrs111033795
openSNPrs111033795
23andMers111033795
23andMe allrs111033795
SNP Nexus

SNPshotrs111033795
SNPdbers111033795
MSV3drs111033795
GWAS Ctlgrs111033795
Max Magnitude0
ClinVar
Risk rs111033795(A;A)
Alt rs111033795(A;A)
Reference rs111033795(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.34649460G>A
CLNSRC ARUP GALT
CLNACC RCV000022243.1,