{{Rsnum
|rsid=111033690
|Gene=GALT
|Chromosome=9
|position=34647858
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GALT
}}{{omim
|id=606999
|rsnum=111033690
|variant=0010
}}{{ClinVar
|rsid=111033690
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=34647855
|CHROM=9
|GMAF=0.0018
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=GALT:2592
|GENE_NAME=GALT
|GENE_ID=2592
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000009.11:g.34647855C>G; NC_000009.11:g.34647855C>T
|CLNSRC=Emory University; GTR; NCBI curation; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=757; GTR000500501; GTR000500512; 111033690; 606999.0010
|CLNCUI=.,C0268151; C0268151
|CLNDBN=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|Disease=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|CLNACC=RCV000022105.1; RCV000003802.1; RCV000078220.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1518:C0268151:230400:352:79239:124354006
|CLNSIG=5
|COMMON=1
}}