{{Rsnum
|rsid=2070863
|Gene=SERPINF2
|Chromosome=17
|position=1745208
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.1915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SERPINF2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 56.6 | 37.2 | 6.2
| HCB | 76.6 | 19.0 | 4.4
| JPT | 58.4 | 34.5 | 7.1
| YRI | 63.3 | 34.7 | 2.0
| ASW | 64.9 | 35.1 | 0.0
| CHB | 76.6 | 19.0 | 4.4
| CHD | 62.4 | 33.0 | 4.6
| GIH | 30.7 | 55.4 | 13.9
| LWK | 60.0 | 33.6 | 6.4
| MEX | 65.5 | 32.8 | 1.7
| MKK | 54.5 | 40.4 | 5.1
| TSI | 75.5 | 20.6 | 3.9
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2070863
|allele=T
|frequency=0.233
|uid=1103645260004
|type=heterozygous_SNP
|hugo=SERPINF2
|ensembl gene=ENSG00000167711
|ensembl transcript=ENST00000324015
|sift=
|disease=Defects in SERPINF2 are the cause of alpha-2-plasmin inhibitor deficiency (MIM:262850); a disease resulting in severe hemorrhagic diathesis.
}}

{{GET Evidence
|gene=SERPINF2
|aa_change=Arg33Trp
|aa_change_short=R33W
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2070863
|overall_frequency_n=2131
|overall_frequency_d=10614
|overall_frequency=0.200773
|n_genomes=16
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.311
|nblosum100=7
|autoscore=0
|webscore=N
}}

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