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rs111033677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033677(A;A)
Make rs111033677(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647665
GeneGALT
is asnp
is mentioned by
dbSNPrs111033677
ebirs111033677
HLIrs111033677
Exacrs111033677
Varsomers111033677
Maprs111033677
PheGenIrs111033677
hapmaprs111033677
1000 genomesrs111033677
hgdprs111033677
ensemblrs111033677
gopubmedrs111033677
geneviewrs111033677
scholarrs111033677
googlers111033677
pharmgkbrs111033677
gwascentralrs111033677
openSNPrs111033677
23andMers111033677
23andMe allrs111033677
SNP Nexus

SNPshotrs111033677
SNPdbers111033677
MSV3drs111033677
GWAS Ctlgrs111033677
Max Magnitude0
ClinVar
Risk rs111033677(A;A)
Alt rs111033677(A;A)
Reference rs111033677(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.34647662G>A
CLNSRC ARUP GALT
CLNACC RCV000022089.1,