{{Rsnum
|rsid=1446495
|Gene=DPP10
|Chromosome=2
|position=115768384
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.02938
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DPP10
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 27.2 | 71.4
| ASW | 1.8 | 12.3 | 86.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 1.8 | 18.3 | 79.8
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 6.4 | 93.6
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1446495
|allele=A
|frequency=1
|uid=1103658192097
|type=homozygous_SNP
|hugo=DPP10
|ensembl gene=ENSG00000175497
|ensembl transcript=ENST00000310323
|sift=TOLERATED
|disease=Defects in DPP10 may be a cause of susceptibility to asthma. Defects in splicing have been observed.
}}

{{GET Evidence
|gene=DPP10
|aa_change=Val405Ile
|aa_change_short=V405I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1446495
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=1
|webscore=N
}}

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