{{Rsnum
|rsid=25651
|Gene=ANPEP
|Chromosome=15
|position=89792557
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3154
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ANPEP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 49.6 | 43.4
| HCB | 5.9 | 44.1 | 50.0
| JPT | 1.8 | 34.5 | 63.7
| YRI | 35.4 | 49.0 | 15.6
| ASW | 24.6 | 49.1 | 26.3
| CHB | 5.9 | 44.1 | 50.0
| CHD | 4.6 | 37.6 | 57.8
| GIH | 12.9 | 45.5 | 41.6
| LWK | 19.1 | 52.7 | 28.2
| MEX | 5.3 | 42.1 | 52.6
| MKK | 21.2 | 53.8 | 25.0
| TSI | 10.8 | 37.3 | 52.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=25651
|allele=T
|frequency=0.288
|uid=1103645680856
|type=heterozygous_SNP
|hugo=ANPEP
|ensembl gene=ENSG00000166825
|ensembl transcript=ENST00000300060
|sift=TOLERATED
|disease=Defects in ANPEP may be a cause of various types of leukemia or lymphoma.
}}

{{PMID Auto
|PMID=18682748
|Title=Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.
|OA=1
}}

{{PMID Auto
|PMID=21881118
|Title=Genetic variants and susceptibility to neurological complications following West Nile virus infection.
|OA=1
}}

{{GET Evidence
|gene=ANPEP
|aa_change=Ser752Asn
|aa_change_short=S752N
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs25651
|overall_frequency_n=4083
|overall_frequency_d=10758
|overall_frequency=0.379532
|n_genomes=35
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}