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rs111033781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033781(A;A)
Make rs111033781(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649058
GeneGALT
is asnp
is mentioned by
dbSNPrs111033781
ebirs111033781
HLIrs111033781
Exacrs111033781
Varsomers111033781
Maprs111033781
PheGenIrs111033781
hapmaprs111033781
1000 genomesrs111033781
hgdprs111033781
ensemblrs111033781
gopubmedrs111033781
geneviewrs111033781
scholarrs111033781
googlers111033781
pharmgkbrs111033781
gwascentralrs111033781
openSNPrs111033781
23andMers111033781
23andMe allrs111033781
SNP Nexus

SNPshotrs111033781
SNPdbers111033781
MSV3drs111033781
GWAS Ctlgrs111033781
Max Magnitude0
ClinVar
Risk rs111033781(A;A)
Alt rs111033781(A;A)
Reference rs111033781(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.34649055T>A
CLNSRC ARUP GALT
CLNACC RCV000022226.1,