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rs367543264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367543264(A;A)
Make rs367543264(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position34649086
GeneGALT
is asnp
is mentioned by
dbSNPrs367543264
ebirs367543264
HLIrs367543264
Exacrs367543264
Varsomers367543264
Maprs367543264
PheGenIrs367543264
hapmaprs367543264
1000 genomesrs367543264
hgdprs367543264
ensemblrs367543264
gopubmedrs367543264
geneviewrs367543264
scholarrs367543264
googlers367543264
pharmgkbrs367543264
gwascentralrs367543264
openSNPrs367543264
23andMers367543264
23andMe allrs367543264
SNP Nexus

SNPshotrs367543264
SNPdbers367543264
MSV3drs367543264
GWAS Ctlgrs367543264
Max Magnitude0
ClinVar
Risk rs367543264(A;A)
Alt rs367543264(A;A)
Reference rs367543264(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.34649083G>A
CLNSRC ARUP GALT
CLNACC RCV000022230.1,