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rs111033775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033775(G;G)
Make rs111033775(G;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649043
GeneGALT
is asnp
is mentioned by
dbSNPrs111033775
ebirs111033775
HLIrs111033775
Exacrs111033775
Varsomers111033775
Maprs111033775
PheGenIrs111033775
hapmaprs111033775
1000 genomesrs111033775
hgdprs111033775
ensemblrs111033775
gopubmedrs111033775
geneviewrs111033775
scholarrs111033775
googlers111033775
pharmgkbrs111033775
gwascentralrs111033775
openSNPrs111033775
23andMers111033775
23andMe allrs111033775
SNP Nexus

SNPshotrs111033775
SNPdbers111033775
MSV3drs111033775
GWAS Ctlgrs111033775
Max Magnitude0
ClinVar
Risk rs111033775(G;G)
Alt rs111033775(G;G)
Reference rs111033775(T;T)
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.34649040T>G
CLNSRC ARUP GALT
CLNACC RCV000022222.1,