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rs111033779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033779(G;G)
Make rs111033779(G;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649013
GeneGALT
is asnp
is mentioned by
dbSNPrs111033779
ClinGenrs111033779
ebirs111033779
HLIrs111033779
Exacrs111033779
Varsomers111033779
Maprs111033779
PheGenIrs111033779
hapmaprs111033779
1000 genomesrs111033779
hgdprs111033779
ensemblrs111033779
gopubmedrs111033779
geneviewrs111033779
scholarrs111033779
googlers111033779
pharmgkbrs111033779
gwascentralrs111033779
openSNPrs111033779
23andMers111033779
23andMe allrs111033779
SNP Nexus

SNPshotrs111033779
SNPdbers111033779
MSV3drs111033779
GWAS Ctlgrs111033779
Max Magnitude0
ClinVar
Risk rs111033779(G;G)
Alt rs111033779(G;G)
Reference Rs111033779(T;T)
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.34649010T>G
CLNSRC ARUP GALT
CLNACC RCV000022217.1,