{{Rsnum
|rsid=146187042
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=C8B
|position=56956889
|Gene_s=C8B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000029239.26
|CLNALLE=1
|CLNDBN=Complement component 8 deficiency type 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151080:613789
|CLNHGVS=NC_000001.11:g.56956889G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000066.2:c.271C>T; 120960.0004
|Disease=Complement component 8 deficiency type 2
|FwdALT=A
|FwdREF=G
|GENEINFO=C8B:732
|GENE_ID=732
|GENE_NAME=C8B
|REF=G
|RSPOS=56956889
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000605000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=146187042
|CLNORIGIN=1
}}