{{Rsnum
|rsid=121913553
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PLOD1
|position=11970750
|Gene_s=PLOD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=153454
|rsnum=121913553
|variant=0009
}}{{ClinVar
|rsid=121913553
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=11970750
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=PLOD1:5351
|GENE_NAME=PLOD1
|GENE_ID=5351
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11970750G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000302.3:c.1836G>C; 153454.0009
|CLNSIG=5
|CLNCUI=C0268342
|CLNDBN=Ehlers-Danlos syndrome, hydroxylysine-deficient
|Disease=Ehlers-Danlos syndrome
|CLNACC=RCV000015449.24
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1462:C0268342:225400:ORPHA1900:25606004
}}