{{Rsnum
|rsid=137852900
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GNPTAB
|position=101770185
|Gene_s=GNPTAB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607840
|variant=0015
|rsnum=137852900
}}{{ClinVar
|rsid=137852900
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=102163963
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=GNPTAB:79158
|GENE_NAME=GNPTAB
|GENE_ID=79158
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.102163963A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1828; 607840.0015
|CLNSIG=5
|CLNCUI=C0033788; C2673377
|CLNDBN=Pseudo-Hurler polydystrophy; I cell disease
|Disease=Pseudo-Hurler polydystrophy; I cell disease
|CLNACC=RCV000002904.1; RCV000002905.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1828:NBK1875:C0033788:252600:577:65764006; NBK1828:NBK1875:C2673377:252500:576
}}{{PMID Auto
|PMID=19197337
|Title=Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype-phenotype correlation.
}}