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

rs111033755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033755(A;G)
Make rs111033755(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34648826
GeneGALT
is asnp
is mentioned by
dbSNPrs111033755
ebirs111033755
HLIrs111033755
Exacrs111033755
Varsomers111033755
Maprs111033755
PheGenIrs111033755
hapmaprs111033755
1000 genomesrs111033755
hgdprs111033755
ensemblrs111033755
gopubmedrs111033755
geneviewrs111033755
scholarrs111033755
googlers111033755
pharmgkbrs111033755
gwascentralrs111033755
openSNPrs111033755
23andMers111033755
23andMe allrs111033755
SNP Nexus

SNPshotrs111033755
SNPdbers111033755
MSV3drs111033755
GWAS Ctlgrs111033755
Max Magnitude0
ClinVar
Risk rs111033755(C,G;C,G)
Alt rs111033755(C,G;C,G)
Reference rs111033755(A;A)
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.34648823A>C; NC_000009.11:g.34648823A>G
CLNSRC ARUP GALT
CLNACC RCV000022193.1, RCV000022192.1,