Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033825

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs111033825(-;-)
Make rs111033825(-;G)
Make rs111033825(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648427
GeneGALT
is asnp
is mentioned by
dbSNPrs111033825
ebirs111033825
HLIrs111033825
Exacrs111033825
Varsomers111033825
Maprs111033825
PheGenIrs111033825
hapmaprs111033825
1000 genomesrs111033825
hgdprs111033825
ensemblrs111033825
gopubmedrs111033825
geneviewrs111033825
scholarrs111033825
googlers111033825
pharmgkbrs111033825
gwascentralrs111033825
openSNPrs111033825
23andMers111033825
23andMe allrs111033825
SNP Nexus

SNPshotrs111033825
SNPdbers111033825
MSV3drs111033825
GWAS Ctlgrs111033825
Max Magnitude0
ClinVar
Risk rs111033825(G;G)
Alt rs111033825(G;G)
Reference rs111033825(;)
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.34648424dupG
CLNSRC ClinVar
CLNACC RCV000022177.1,