{{Rsnum
|rsid=150022116
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=C8B
|position=56956799
|Gene_s=C8B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=1
|CLNACC=RCV000029238.26
|CLNALLE=1
|CLNDBN=Complement component 8 deficiency type 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151080:613789
|CLNHGVS=NC_000001.11:g.56956799G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000066.2:c.361C>T; 120960.0003
|Disease=Complement component 8 deficiency type 2
|FwdALT=A,T
|FwdREF=G
|GENEINFO=C8B:732
|GENE_ID=732
|GENE_NAME=C8B
|REF=G
|RSPOS=56956799
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSN;REF;SYN;ASP;VLD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000705040002110100
|WGT=1
|dbSNPBuildID=134
|rsid=150022116
|CLNORIGIN=1
}}