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rs111033774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033774(C;T)
Make rs111033774(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649042
GeneGALT
is asnp
is mentioned by
dbSNPrs111033774
ebirs111033774
HLIrs111033774
Exacrs111033774
Varsomers111033774
Maprs111033774
PheGenIrs111033774
hapmaprs111033774
1000 genomesrs111033774
hgdprs111033774
ensemblrs111033774
gopubmedrs111033774
geneviewrs111033774
scholarrs111033774
googlers111033774
pharmgkbrs111033774
gwascentralrs111033774
openSNPrs111033774
23andMers111033774
23andMe allrs111033774
SNP Nexus

SNPshotrs111033774
SNPdbers111033774
MSV3drs111033774
GWAS Ctlgrs111033774
Max Magnitude0
ClinVar
Risk rs111033774(T;T)
Alt rs111033774(T;T)
Reference rs111033774(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.34649039C>T
CLNSRC ARUP GALT
CLNACC RCV000022221.1,