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rs111033699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033699(C;C)
Make rs111033699(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647902
GeneGALT
is asnp
is mentioned by
dbSNPrs111033699
ebirs111033699
HLIrs111033699
Exacrs111033699
Varsomers111033699
Maprs111033699
PheGenIrs111033699
hapmaprs111033699
1000 genomesrs111033699
hgdprs111033699
ensemblrs111033699
gopubmedrs111033699
geneviewrs111033699
scholarrs111033699
googlers111033699
pharmgkbrs111033699
gwascentralrs111033699
openSNPrs111033699
23andMers111033699
23andMe allrs111033699
SNP Nexus

SNPshotrs111033699
SNPdbers111033699
MSV3drs111033699
GWAS Ctlgrs111033699
Max Magnitude0
ClinVar
Risk rs111033699(C;C)
Alt rs111033699(C;C)
Reference rs111033699(G;G)
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.34647899G>C
CLNSRC ARUP GALT
CLNACC RCV000022115.1,