{{Rsnum
|rsid=121434414
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PLOD3
|position=101215100
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PLOD3
}}{{omim
|id=603066
|rsnum=121434414
|variant=0001
}}{{ClinVar
|rsid=121434414
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=100858381
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PLOD3:8985
|GENE_NAME=PLOD3
|GENE_ID=8985
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100858381T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603066.0001
|CLNSIG=5
|CLNCUI=C2676285
|CLNDBN=Bone fragility with contractures, arterial rupture, and deafness
|Disease=Bone fragility with contractures
|CLNACC=RCV000007022.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2676285:612394
}}