{{Rsnum
|rsid=121964919
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=C7
|position=40979809
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C7
}}{{omim
|id=217070
|rsnum=121964919
|variant=0001
}}{{ClinVar
|rsid=121964919
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=40979911
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=C7:730
|GENE_NAME=C7
|GENE_ID=730
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.40979911T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=217070.0001
|CLNSIG=5
|CLNCUI=C1864694
|CLNDBN=Complement component 7 deficiency
|Disease=Complement component 7 deficiency
|CLNACC=RCV000012885.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1864694:610102
}}