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rs111033664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033664(C;T)
Make rs111033664(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647244
GeneGALT
is asnp
is mentioned by
dbSNPrs111033664
ebirs111033664
HLIrs111033664
Exacrs111033664
Varsomers111033664
Maprs111033664
PheGenIrs111033664
hapmaprs111033664
1000 genomesrs111033664
hgdprs111033664
ensemblrs111033664
gopubmedrs111033664
geneviewrs111033664
scholarrs111033664
googlers111033664
pharmgkbrs111033664
gwascentralrs111033664
openSNPrs111033664
23andMers111033664
23andMe allrs111033664
SNP Nexus

SNPshotrs111033664
SNPdbers111033664
MSV3drs111033664
GWAS Ctlgrs111033664
Max Magnitude0
ClinVar
Risk rs111033664(T;T)
Alt rs111033664(T;T)
Reference rs111033664(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.34647241C>T
CLNSRC ARUP GALT
CLNACC RCV000022070.1,