Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033746(C;T)
Make rs111033746(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648403
GeneGALT
is asnp
is mentioned by
dbSNPrs111033746
ebirs111033746
HLIrs111033746
Exacrs111033746
Varsomers111033746
Maprs111033746
PheGenIrs111033746
hapmaprs111033746
1000 genomesrs111033746
hgdprs111033746
ensemblrs111033746
gopubmedrs111033746
geneviewrs111033746
scholarrs111033746
googlers111033746
pharmgkbrs111033746
gwascentralrs111033746
openSNPrs111033746
23andMers111033746
23andMe allrs111033746
SNP Nexus

SNPshotrs111033746
SNPdbers111033746
MSV3drs111033746
GWAS Ctlgrs111033746
Max Magnitude0
ClinVar
Risk rs111033746(T;T)
Alt rs111033746(T;T)
Reference rs111033746(C;C)
Significance Other
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.34648400C>T
CLNSRC ARUP GALT HGMD
CLNACC RCV000022170.6,