{{Rsnum
|rsid=104893743
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HYAL1
|position=50302155
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HYAL1
}}{{omim
|id=607071
|rsnum=104893743
|variant=0001
}}{{ClinVar
|rsid=104893743
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50339586
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HYAL1:3373
|GENE_NAME=HYAL1
|GENE_ID=3373
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.50339586C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607071.0001
|CLNSIG=5
|CLNCUI=C1291490
|CLNDBN=Deficiency of hyaluronoglucosaminidase
|Disease=Deficiency of hyaluronoglucosaminidase
|CLNACC=RCV000003708.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1291490:601492:67041:124473006
}}