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rs111033824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033824(C;C)
Make rs111033824(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position34650447
GeneGALT, IL11RA
is asnp
is mentioned by
dbSNPrs111033824
ebirs111033824
HLIrs111033824
Exacrs111033824
Varsomers111033824
Maprs111033824
PheGenIrs111033824
hapmaprs111033824
1000 genomesrs111033824
hgdprs111033824
ensemblrs111033824
gopubmedrs111033824
geneviewrs111033824
scholarrs111033824
googlers111033824
pharmgkbrs111033824
gwascentralrs111033824
openSNPrs111033824
23andMers111033824
23andMe allrs111033824
SNP Nexus

SNPshotrs111033824
SNPdbers111033824
MSV3drs111033824
GWAS Ctlgrs111033824
Max Magnitude0
ClinVar
Risk rs111033824(C;C)
Alt rs111033824(C;C)
Reference rs111033824(T;T)
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.34650444T>C
CLNSRC ARUP GALT
CLNACC RCV000022281.1,