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rs111033769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033769(G;T)
Make rs111033769(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648830
GeneGALT
is asnp
is mentioned by
dbSNPrs111033769
ebirs111033769
HLIrs111033769
Exacrs111033769
Varsomers111033769
Maprs111033769
PheGenIrs111033769
hapmaprs111033769
1000 genomesrs111033769
hgdprs111033769
ensemblrs111033769
gopubmedrs111033769
geneviewrs111033769
scholarrs111033769
googlers111033769
pharmgkbrs111033769
gwascentralrs111033769
openSNPrs111033769
23andMers111033769
23andMe allrs111033769
SNP Nexus

SNPshotrs111033769
SNPdbers111033769
MSV3drs111033769
GWAS Ctlgrs111033769
Max Magnitude0
ClinVar
Risk rs111033769(T;T)
Alt rs111033769(T;T)
Reference rs111033769(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.34648827G>T
CLNSRC ARUP GALT
CLNACC RCV000022195.1,