{{Rsnum
|rsid=121909592
|Gene=C9
|Chromosome=5
|position=39341276
|Orientation=plus
|GMAF=0.003673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=C9
}}{{omim
|id=120940
|rsnum=121909592
|variant=0001
}}{{ClinVar
|rsid=121909592
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=39341378
|CHROM=5
|GMAF=0.0037
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000416110100
|GENEINFO=C9:735
|GENE_NAME=C9
|GENE_ID=735
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.39341378G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9963; 0.003673
|CLNACC=RCV000018568.26
|CLNDBN=Complement component 9 deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151189:613825
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120940.0001
|COMMON=1
|Disease=Complement component 9 deficiency
}}