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rs111033819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033819(A;G)
Make rs111033819(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34650441
GeneGALT, IL11RA
is asnp
is mentioned by
dbSNPrs111033819
ebirs111033819
HLIrs111033819
Exacrs111033819
Varsomers111033819
Maprs111033819
PheGenIrs111033819
hapmaprs111033819
1000 genomesrs111033819
hgdprs111033819
ensemblrs111033819
gopubmedrs111033819
geneviewrs111033819
scholarrs111033819
googlers111033819
pharmgkbrs111033819
gwascentralrs111033819
openSNPrs111033819
23andMers111033819
23andMe allrs111033819
SNP Nexus

SNPshotrs111033819
SNPdbers111033819
MSV3drs111033819
GWAS Ctlgrs111033819
Max Magnitude0
ClinVar
Risk rs111033819(G;G)
Alt rs111033819(G;G)
Reference rs111033819(A;A)
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.34650438A>G
CLNSRC ARUP GALT
CLNACC RCV000022280.1,