{{Rsnum
|rsid=121912930
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=COL5A2
|position=189043177
|Gene_s=COL5A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120190
|rsnum=121912930
|variant=0003
}}{{ClinVar
|rsid=121912930
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=189907903
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=COL5A2:1290
|GENE_NAME=COL5A2
|GENE_ID=1290
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.189907903C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120190.0003
|CLNSIG=5
|CLNCUI=C0268336
|CLNDBN=Ehlers-Danlos syndrome, type 2
|Disease=Ehlers-Danlos syndrome
|CLNACC=RCV000018738.22
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1244:C0268336:130010:287:90318:20766005
}}