{{Rsnum
|rsid=34000044
|Gene=C9
|Chromosome=5
|position=39342112
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=C9
}}{{omim
|id=120940
|rsnum=34000044
|variant=0002
}}{{ClinVar
|rsid=34000044
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=39342214
|CHROM=5
|GMAF=0.0009
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050360000000040116110100
|GENEINFO=C9:735
|GENE_NAME=C9
|GENE_ID=735
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000005.9:g.39342214G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNACC=RCV000018569.26
|CLNDBN=Complement component 9 deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151189:613825
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120940.0002
|COMMON=0
|Disease=Complement component 9 deficiency
}}