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rs111033725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033725(C;T)
Make rs111033725(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648163
GeneGALT
is asnp
is mentioned by
dbSNPrs111033725
ebirs111033725
HLIrs111033725
Exacrs111033725
Varsomers111033725
Maprs111033725
PheGenIrs111033725
hapmaprs111033725
1000 genomesrs111033725
hgdprs111033725
ensemblrs111033725
gopubmedrs111033725
geneviewrs111033725
scholarrs111033725
googlers111033725
pharmgkbrs111033725
gwascentralrs111033725
openSNPrs111033725
23andMers111033725
23andMe allrs111033725
SNP Nexus

SNPshotrs111033725
SNPdbers111033725
MSV3drs111033725
GWAS Ctlgrs111033725
Max Magnitude0
ClinVar
Risk rs111033725(T;T)
Alt rs111033725(T;T)
Reference rs111033725(C;C)
Significance Pathogenic
Disease Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Variation info
Gene GALT
CLNDBN Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Reversed 0
HGVS NC_000009.11:g.34648160C>T
CLNSRC ARUP GALT
CLNACC RCV000022150.1, RCV000224017.1,