{{Rsnum
|rsid=121909582
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C1S
|position=7070184
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C1S
}}{{omim
|id=120580
|rsnum=121909582
|variant=0002
}}{{ClinVar
|rsid=121909582
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=7177488
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=C1S:716
|GENE_NAME=C1S
|GENE_ID=716
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.7177488C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000018597.22
|CLNDBN=Complement 1s deficiency
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0398755:234598004
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120580.0002
|Disease=Complement 1s deficiency
}}