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rs111033786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033786(A;G)
Make rs111033786(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649455
GeneGALT
is asnp
is mentioned by
dbSNPrs111033786
ebirs111033786
HLIrs111033786
Exacrs111033786
Varsomers111033786
Maprs111033786
PheGenIrs111033786
hapmaprs111033786
1000 genomesrs111033786
hgdprs111033786
ensemblrs111033786
gopubmedrs111033786
geneviewrs111033786
scholarrs111033786
googlers111033786
pharmgkbrs111033786
gwascentralrs111033786
openSNPrs111033786
23andMers111033786
23andMe allrs111033786
SNP Nexus

SNPshotrs111033786
SNPdbers111033786
MSV3drs111033786
GWAS Ctlgrs111033786
Max Magnitude0
ClinVar
Risk rs111033786(G;G)
Alt rs111033786(G;G)
Reference rs111033786(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.34649452A>G
CLNSRC ARUP GALT
CLNACC RCV000022238.1,