{{Rsnum
|rsid=121912503
|Chromosome=6
|position=160650438
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LPA
|Gene_s=LPA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152200
|rsnum=121912503
|variant=0004
}}{{ClinVar
|rsid=121912503
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=161071470
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=LPA:4018
|GENE_NAME=LPA
|GENE_ID=4018
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.161071470G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015535.24
|CLNDBN=LIPOPROTEIN(a) DEFICIENCY, CONGENITAL
|CLNDSDB=MedGen
|CLNDSDBID=C1835362
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=152200.0004
|Disease=LIPOPROTEIN(a) DEFICIENCY
}}