{{Rsnum
|rsid=398122868
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GGCTGTG)
|geno3=(GGCTGTG;GGCTGTG)
|Gene=C8B
|position=56945878
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GCACAGCC
|CHROM=1
|CLNACC=RCV000029242.22
|CLNALLE=1
|CLNDBN=Complement component 8 deficiency type 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151080:613789
|CLNHGVS=NC_000001.11:g.56945879_56945885dupCACAGCC
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000066.3:c.1041_1047dupGGCTGTG; 120960.0007
|Disease=Complement component 8 deficiency type 2
|FwdALT=GGCTGTG
|REF=G
|RSPOS=56945878
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060001205000002110200
|WGT=1
|dbSNPBuildID=138
|rsid=398122868
|CLNORIGIN=1
|GENEINFO=C8B:732
|GENE_ID=732
|GENE_NAME=C8B
}}