{{Rsnum
|rsid=2824721
|Gene=TMPRSS15
|Chromosome=21
|position=18297801
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.2966
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 60.2 | 38.1 | 1.8
| HCB | 38.0 | 48.2 | 13.9
| JPT | 54.0 | 37.2 | 8.8
| YRI | 42.9 | 46.9 | 10.2
| ASW | 50.9 | 42.1 | 7.0
| CHB | 38.0 | 48.2 | 13.9
| CHD | 45.4 | 49.1 | 5.6
| GIH | 54.5 | 39.6 | 5.9
| LWK | 41.7 | 44.4 | 13.9
| MEX | 55.2 | 37.9 | 6.9
| MKK | 31.6 | 56.8 | 11.6
| TSI | 57.8 | 37.3 | 4.9
| HapMapRevision=28
}}{{Venter SNP
|rsid=2824721
|allele=A
|frequency=0.792
|uid=1103643081453
|type=homozygous_SNP
|hugo=PRSS7
|ensembl gene=ENSG00000154646
|ensembl transcript=ENST00000284885
|sift=TOLERATED
|disease=Defects in PRSS7 are a cause of enterokinase deficiency (MIM:226200); a life-threatening intestinal malabsorption disorder characterized by diarrhea and failure to thrive.
}}

{{GET Evidence
|gene=TMPRSS15
|aa_change=Pro732Ser
|aa_change_short=P732S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2824721
|overall_frequency_n=8111
|overall_frequency_d=10756
|overall_frequency=0.754091
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=80
|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 | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}