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rs111033809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033809(A;G)
Make rs111033809(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649506
GeneGALT
is asnp
is mentioned by
dbSNPrs111033809
ebirs111033809
HLIrs111033809
Exacrs111033809
Varsomers111033809
Maprs111033809
PheGenIrs111033809
hapmaprs111033809
1000 genomesrs111033809
hgdprs111033809
ensemblrs111033809
gopubmedrs111033809
geneviewrs111033809
scholarrs111033809
googlers111033809
pharmgkbrs111033809
gwascentralrs111033809
openSNPrs111033809
23andMers111033809
23andMe allrs111033809
SNP Nexus

SNPshotrs111033809
SNPdbers111033809
MSV3drs111033809
GWAS Ctlgrs111033809
Max Magnitude0
ClinVar
Risk rs111033809(G;G)
Alt rs111033809(G;G)
Reference rs111033809(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.34649503A>G
CLNSRC ARUP GALT
CLNACC RCV000022260.1,