{{Rsnum
|rsid=4972946
|Gene=SP140
|Chromosome=2
|position=230284393
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.03949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SP140
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 83.2 | 16.8 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 91.2 | 8.8 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 91.2 | 8.8 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=4972946
|allele=A
|frequency=0.119
|uid=1103658390755
|type=heterozygous_SNP
|hugo=SP140
|ensembl gene=ENSG00000079263
|ensembl transcript=ENST00000181092
|sift=TOLERATED
|disease=This antigen is recognized by autoantibodies from patients with primary biliary cirrhosis.
}}

{{GET Evidence
|gene=SP140
|aa_change=Glu516Lys
|aa_change_short=E516K
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4972946
|overall_frequency_n=9163
|overall_frequency_d=9748
|overall_frequency=0.939988
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=106
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}