{{Rsnum
|rsid=121909116
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ECM1
|position=150510989
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ECM1
}}{{omim
|id=602201
|rsnum=121909116
|variant=0006
}}{{ClinVar
|rsid=121909116
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=150510989
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=ECM1:1893
|GENE_NAME=ECM1
|GENE_ID=1893
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.150510989T>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004425.3:c.499T>A; 602201.0006
|CLNSIG=5
|CLNCUI=C0023795
|CLNDBN=Lipid proteinosis
|Disease=Lipid proteinosis
|CLNACC=RCV000007902.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0023795:247100:ORPHA530:38692000
}}