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rs111033723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033723(A;A)
Make rs111033723(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648172
GeneGALT
is asnp
is mentioned by
dbSNPrs111033723
ebirs111033723
HLIrs111033723
Exacrs111033723
Varsomers111033723
Maprs111033723
PheGenIrs111033723
hapmaprs111033723
1000 genomesrs111033723
hgdprs111033723
ensemblrs111033723
gopubmedrs111033723
geneviewrs111033723
scholarrs111033723
googlers111033723
pharmgkbrs111033723
gwascentralrs111033723
openSNPrs111033723
23andMers111033723
23andMe allrs111033723
SNP Nexus

SNPshotrs111033723
SNPdbers111033723
MSV3drs111033723
GWAS Ctlgrs111033723
Max Magnitude0
ClinVar
Risk rs111033723(A;A)
Alt rs111033723(A;A)
Reference rs111033723(G;G)
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.34648169G>A
CLNSRC ARUP GALT
CLNACC RCV000022151.1,