{{Rsnum
|rsid=2086310
|Gene=ADAMTS16
|Chromosome=5
|position=5146222
|Orientation=minus
|GMAF=0.3122
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ADAMTS16
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 54.7 | 39.1 | 6.2
| HCB | 24.4 | 44.4 | 31.1
| JPT | 36.4 | 47.7 | 15.9
| YRI | 28.8 | 54.2 | 16.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 24.4 | 44.4 | 31.1
| 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
}}{{omim
|desc=A DISINTEGRIN-LIKE AND METALLOPROTEINASE WITH THROMBOSPONDIN TYPE
|id=607510
|rsnum=2086310
}}

{{omim
|id=610262
|rsnum=2086310
}}

{{PMID Auto
|PMID=19423552
|Title=Positional identification of variants of Adamts16 linked to inherited hypertension.
|OA=1
}}

{{GET Evidence
|gene=ADAMTS16
|aa_change=Pro90Ala
|aa_change_short=P90A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2086310
|overall_frequency_n=7753
|overall_frequency_d=10188
|overall_frequency=0.760993
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

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