{{Rsnum
|rsid=121912954
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MMP2
|position=55485677
|Gene_s=MMP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120360
|rsnum=121912954
|variant=0002
}}{{ClinVar
|rsid=121912954
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=55519589
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MMP2:4313
|GENE_NAME=MMP2
|GENE_ID=4313
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.55519589C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120360.0002
|CLNSIG=5
|CLNCUI=C1850155
|CLNDBN=Torg Winchester syndrome
|Disease=Torg Winchester syndrome
|CLNACC=RCV000018644.27
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850155:259600:3460
}}