{{Rsnum
|rsid=2824790
|Gene=TMPRSS15
|Chromosome=21
|position=18383723
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|GMAF=0.2392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TMPRSS15
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 33.8 | 53.8 | 12.3
| HCB | 88.9 | 8.9 | 2.2
| JPT | 75.0 | 25.0 | 0.0
| YRI | 54.0 | 41.3 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 88.9 | 8.9 | 2.2
| 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
}}{{Venter SNP
|rsid=2824790
|allele=G
|frequency=0.375
|uid=1103643081599
|type=homozygous_SNP
|hugo=PRSS7
|ensembl gene=ENSG00000154646
|ensembl transcript=ENST00000284885
|sift=AFFECT FUNCTION
|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=Glu134Gln
|aa_change_short=E134Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2824790
|overall_frequency_n=2924
|overall_frequency_d=10758
|overall_frequency=0.271798
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.075
|nblosum100=-2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}