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rs111033822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033822(A;A)
Make rs111033822(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position34650407
GeneGALT, IL11RA
is asnp
is mentioned by
dbSNPrs111033822
ebirs111033822
HLIrs111033822
Exacrs111033822
Varsomers111033822
Maprs111033822
PheGenIrs111033822
hapmaprs111033822
1000 genomesrs111033822
hgdprs111033822
ensemblrs111033822
gopubmedrs111033822
geneviewrs111033822
scholarrs111033822
googlers111033822
pharmgkbrs111033822
gwascentralrs111033822
openSNPrs111033822
23andMers111033822
23andMe allrs111033822
SNP Nexus

SNPshotrs111033822
SNPdbers111033822
MSV3drs111033822
GWAS Ctlgrs111033822
Max Magnitude0
ClinVar
Risk rs111033822(A;A)
Alt rs111033822(A;A)
Reference rs111033822(C;C)
Significance Pathogenic
Disease Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Variation info
Gene GALT IL11RA
CLNDBN Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Reversed 0
HGVS NC_000009.11:g.34650404C>A
CLNSRC ARUP GALT
CLNACC RCV000022278.1,