{{Rsnum
|rsid=121909581
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C1QA
|position=22639291
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C1QA
}}{{omim
|id=120550
|rsnum=121909581
|variant=0001
}}{{ClinVar
|rsid=121909581
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=22639291
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=C1QA:712
|GENE_NAME=C1QA
|GENE_ID=712
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.22639291C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_015991.2:c.622C>T; 120550.0001
|CLNSIG=5
|CLNCUI=C3150902
|CLNDBN=C1q deficiency
|Disease=C1q deficiency
|CLNACC=RCV000018602.26
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3150902:613652
}}