{{Rsnum
|rsid=121909593
|Chromosome=5
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=C9
|position=39341267
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C9
}}{{omim
|id=120940
|rsnum=121909593
|variant=0003
}}{{ClinVar
|rsid=121909593
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=39341369
|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.39341369A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018570.26
|CLNDBN=Complement component 9 deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151189:613825
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120940.0003
|Disease=Complement component 9 deficiency
}}