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rs111033829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033829(A;A)
Make rs111033829(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647104
GeneGALT
is asnp
is mentioned by
dbSNPrs111033829
ebirs111033829
HLIrs111033829
Exacrs111033829
Varsomers111033829
Maprs111033829
PheGenIrs111033829
hapmaprs111033829
1000 genomesrs111033829
hgdprs111033829
ensemblrs111033829
gopubmedrs111033829
geneviewrs111033829
scholarrs111033829
googlers111033829
pharmgkbrs111033829
gwascentralrs111033829
openSNPrs111033829
23andMers111033829
23andMe allrs111033829
SNP Nexus

SNPshotrs111033829
SNPdbers111033829
MSV3drs111033829
GWAS Ctlgrs111033829
Max Magnitude0
ClinVar
Risk rs111033829(A;A)
Alt rs111033829(A;A)
Reference rs111033829(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.34647101G>A
CLNSRC ARUP GALT
CLNACC RCV000022051.1,