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rs111033765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033765(A;G)
Make rs111033765(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648886
GeneGALT
is asnp
is mentioned by
dbSNPrs111033765
ebirs111033765
HLIrs111033765
Exacrs111033765
Varsomers111033765
Maprs111033765
PheGenIrs111033765
hapmaprs111033765
1000 genomesrs111033765
hgdprs111033765
ensemblrs111033765
gopubmedrs111033765
geneviewrs111033765
scholarrs111033765
googlers111033765
pharmgkbrs111033765
gwascentralrs111033765
openSNPrs111033765
23andMers111033765
23andMe allrs111033765
SNP Nexus

SNPshotrs111033765
SNPdbers111033765
MSV3drs111033765
GWAS Ctlgrs111033765
Max Magnitude0
ClinVar
Risk rs111033765(G;G)
Alt rs111033765(G;G)
Reference rs111033765(A;A)
Significance Pathogenic
Disease Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Variation info
Gene GALT
CLNDBN Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Reversed 0
HGVS NC_000009.11:g.34648883A>G
CLNSRC ARUP GALT
CLNACC RCV000022208.1, RCV000180101.1,