{{Rsnum
|rsid=2509897
|Chromosome=11
|position=57595144
|Orientation=minus
|GMAF=0.2222
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 48.1 | 33.3 | 18.5
| HCB | 83.3 | 16.7 | 0.0
| JPT | 78.0 | 17.1 | 4.9
| YRI | 86.9 | 11.5 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 83.3 | 16.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2509897
|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=PA162356025
}}

{{PMID Auto
|PMID=20161815
|Title=SERPING1 polymorphisms in polypoidal choroidal vasculopathy
|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.

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2509897
|overall_frequency_n=92
|overall_frequency_d=128
|overall_frequency=0.71875
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=84
|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 | HumanOmni1Quad}}