{{Rsnum
|rsid=41286844
|Gene=C8B
|Chromosome=1
|position=56940965
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=C8B
}}{{omim
|id=120960
|rsnum=41286844
|variant=0001
}}

{{ClinVar
|rsid=41286844
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=56940965
|CHROM=1
|GMAF=0.0014
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050260000000040116110100
|GENEINFO=C8B:732
|GENE_NAME=C8B
|GENE_ID=732
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.56940965G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000066.2:c.1282C>T; 120960.0001
|CLNSIG=5
|CLNCUI=C3151080
|CLNDBN=Complement component 8 deficiency type 2
|Disease=Complement component 8 deficiency type 2
|CLNACC=RCV000018566.26
|Tags=PM;S3D;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151080:613789
|COMMON=0
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}