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rs111033661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033661(A;G)
Make rs111033661(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647490
GeneGALT
is asnp
is mentioned by
dbSNPrs111033661
ebirs111033661
HLIrs111033661
Exacrs111033661
Varsomers111033661
Maprs111033661
PheGenIrs111033661
hapmaprs111033661
1000 genomesrs111033661
hgdprs111033661
ensemblrs111033661
gopubmedrs111033661
geneviewrs111033661
scholarrs111033661
googlers111033661
pharmgkbrs111033661
gwascentralrs111033661
openSNPrs111033661
23andMers111033661
23andMe allrs111033661
SNP Nexus

SNPshotrs111033661
SNPdbers111033661
MSV3drs111033661
GWAS Ctlgrs111033661
Max Magnitude0
ClinVar
Risk rs111033661(G;G)
Alt rs111033661(G;G)
Reference rs111033661(A;A)
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.34647487A>G
CLNSRC ARUP GALT
CLNACC RCV000022073.4, RCV000185912.1,