{{Rsnum
|rsid=1057335
|Gene=SERPINF2
|Chromosome=17
|position=1754359
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.163
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SERPINF2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 6.3 | 38.7 | 55.0
| HCB | 3.1 | 17.6 | 79.4
| JPT | 7.2 | 36.0 | 56.8
| YRI | 2.8 | 38.7 | 58.5
| ASW | 1.8 | 26.8 | 71.4
| CHB | 3.1 | 17.6 | 79.4
| CHD | 3.8 | 29.2 | 67.0
| GIH | 14.0 | 56.0 | 30.0
| LWK | 2.9 | 26.7 | 70.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 4.5 | 35.5 | 60.0
| TSI | 2.9 | 18.6 | 78.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=1057335
|allele=A
|frequency=0.28
|uid=1103645260030
|type=heterozygous_SNP
|hugo=SERPINF2
|ensembl gene=ENSG00000167711
|ensembl transcript=ENST00000324015
|sift=TOLERATED
|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=Arg434Lys
|aa_change_short=R434K
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1057335
|overall_frequency_n=2032
|overall_frequency_d=10758
|overall_frequency=0.188883
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|nblosum100=-3
|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}}