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

rs111033705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033705(C;T)
Make rs111033705(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647944
GeneGALT
is asnp
is mentioned by
dbSNPrs111033705
ebirs111033705
HLIrs111033705
Exacrs111033705
Varsomers111033705
Maprs111033705
PheGenIrs111033705
hapmaprs111033705
1000 genomesrs111033705
hgdprs111033705
ensemblrs111033705
gopubmedrs111033705
geneviewrs111033705
scholarrs111033705
googlers111033705
pharmgkbrs111033705
gwascentralrs111033705
openSNPrs111033705
23andMers111033705
23andMe allrs111033705
SNP Nexus

SNPshotrs111033705
SNPdbers111033705
MSV3drs111033705
GWAS Ctlgrs111033705
Max Magnitude0
ClinVar
Risk rs111033705(T;T)
Alt rs111033705(T;T)
Reference rs111033705(C;C)
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.34647941C>T
CLNSRC ARUP GALT
CLNACC RCV000022121.1,