{{Rsnum
|rsid=111033663
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GALT
|position=34647227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GALT
}}{{omim
|id=606999
|rsnum=111033663
|variant=0007
}}{{ClinVar
|rsid=111033663
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=34647224
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GALT:2592
|GENE_NAME=GALT
|GENE_ID=2592
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.34647224T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606999.0007
|CLNSIG=5
|CLNCUI=C0268151; C0268151
|CLNDBN=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
|Disease=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
|CLNACC=RCV000003799.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1518:C0268151:230400:352:79239:124354006
}}