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rs111033682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033682(A;G)
Make rs111033682(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647833
GeneGALT
is asnp
is mentioned by
dbSNPrs111033682
ebirs111033682
HLIrs111033682
Exacrs111033682
Varsomers111033682
Maprs111033682
PheGenIrs111033682
hapmaprs111033682
1000 genomesrs111033682
hgdprs111033682
ensemblrs111033682
gopubmedrs111033682
geneviewrs111033682
scholarrs111033682
googlers111033682
pharmgkbrs111033682
gwascentralrs111033682
openSNPrs111033682
23andMers111033682
23andMe allrs111033682
SNP Nexus

SNPshotrs111033682
SNPdbers111033682
MSV3drs111033682
GWAS Ctlgrs111033682
Max Magnitude0
ClinVar
Risk rs111033682(G;G)
Alt rs111033682(G;G)
Reference rs111033682(A;A)
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.34647830A>G
CLNSRC ARUP GALT
CLNACC RCV000022098.1,