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rs111033803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033803(C;T)
Make rs111033803(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649491
GeneGALT
is asnp
is mentioned by
dbSNPrs111033803
ebirs111033803
HLIrs111033803
Exacrs111033803
Varsomers111033803
Maprs111033803
PheGenIrs111033803
hapmaprs111033803
1000 genomesrs111033803
hgdprs111033803
ensemblrs111033803
gopubmedrs111033803
geneviewrs111033803
scholarrs111033803
googlers111033803
pharmgkbrs111033803
gwascentralrs111033803
openSNPrs111033803
23andMers111033803
23andMe allrs111033803
SNP Nexus

SNPshotrs111033803
SNPdbers111033803
MSV3drs111033803
GWAS Ctlgrs111033803
Max Magnitude0
ClinVar
Risk rs111033803(T;T)
Alt rs111033803(T;T)
Reference rs111033803(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.34649488C>T
CLNSRC ARUP GALT
CLNACC RCV000022255.1,