{{Rsnum
|rsid=2511990
|Chromosome=11
|position=57595235
|Orientation=minus
|GMAF=0.3664
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 42.5 | 27.4
| HCB | 78.8 | 20.4 | 0.7
| JPT | 66.4 | 28.3 | 5.3
| YRI | 41.1 | 47.3 | 11.6
| ASW | 28.1 | 49.1 | 22.8
| CHB | 78.8 | 20.4 | 0.7
| CHD | 79.8 | 18.3 | 1.8
| GIH | 26.7 | 48.5 | 24.8
| LWK | 32.7 | 45.5 | 21.8
| MEX | 44.8 | 41.4 | 13.8
| MKK | 35.9 | 47.4 | 16.7
| TSI | 26.5 | 44.1 | 29.4
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2511990
|Name_s=
|Gene_s=SERPING1
|Feature=
|Evidence=PubMed ID:18842294
|Annotation=This variant is associated with age-related macular degeneration.
|Drugs=
|Drug Classes=
|Diseases=Macular Degeneration
|Curation Level=Curated
|PharmGKB Accession ID=PA162356024
}}

{{PMID Auto
|PMID=20062564
|Title=An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population
|OA=1
}}

{{PMID|19169411|OA=1
}} Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects.

{{PMID|20161815|OA=1
}} SERPING1 polymorphisms in polypoidal choroidal vasculopathy.

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2511990
|overall_frequency_n=60
|overall_frequency_d=128
|overall_frequency=0.46875
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=51
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}