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rs111033780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033780(A;A)
Make rs111033780(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649048
GeneGALT
is asnp
is mentioned by
dbSNPrs111033780
ebirs111033780
HLIrs111033780
Exacrs111033780
Varsomers111033780
Maprs111033780
PheGenIrs111033780
hapmaprs111033780
1000 genomesrs111033780
hgdprs111033780
ensemblrs111033780
gopubmedrs111033780
geneviewrs111033780
scholarrs111033780
googlers111033780
pharmgkbrs111033780
gwascentralrs111033780
openSNPrs111033780
23andMers111033780
23andMe allrs111033780
SNP Nexus

SNPshotrs111033780
SNPdbers111033780
MSV3drs111033780
GWAS Ctlgrs111033780
Max Magnitude0
ClinVar
Risk rs111033780(A;A)
Alt rs111033780(A;A)
Reference rs111033780(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.34649045G>A
CLNSRC ARUP GALT
CLNACC RCV000022223.1,