{{Rsnum
|rsid=121909594
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=C9
|position=39306753
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C9
}}{{omim
|id=120940
|rsnum=121909594
|variant=0004
}}{{ClinVar
|rsid=121909594
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=39306855
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=C9:735
|GENE_NAME=C9
|GENE_ID=735
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.39306855G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018571.22
|CLNDBN=Complement component 9 deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151189:613825
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120940.0004
|Disease=Complement component 9 deficiency
}}