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rs111033778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033778(A;A)
Make rs111033778(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649010
GeneGALT
is asnp
is mentioned by
dbSNPrs111033778
ebirs111033778
HLIrs111033778
Exacrs111033778
Varsomers111033778
Maprs111033778
PheGenIrs111033778
hapmaprs111033778
1000 genomesrs111033778
hgdprs111033778
ensemblrs111033778
gopubmedrs111033778
geneviewrs111033778
scholarrs111033778
googlers111033778
pharmgkbrs111033778
gwascentralrs111033778
openSNPrs111033778
23andMers111033778
23andMe allrs111033778
SNP Nexus

SNPshotrs111033778
SNPdbers111033778
MSV3drs111033778
GWAS Ctlgrs111033778
Max Magnitude0
ClinVar
Risk rs111033778(A,C;A,C)
Alt rs111033778(A,C;A,C)
Reference rs111033778(T;T)
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.34649007T>A
CLNSRC ARUP GALT
CLNACC RCV000022216.1,