{{Rsnum
|rsid=1054480
|Gene=ADAMTS2
|Chromosome=5
|position=179113974
|Orientation=minus
|GMAF=0.2521
|Gene_s=ADAMTS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 56.6 | 37.2 | 6.2
| HCB | 51.8 | 42.3 | 5.8
| JPT | 39.8 | 46.9 | 13.3
| YRI | 95.2 | 4.1 | 0.7
| ASW | 78.9 | 21.1 | 0.0
| CHB | 51.8 | 42.3 | 5.8
| CHD | 46.8 | 45.9 | 7.3
| GIH | 39.6 | 45.5 | 14.9
| LWK | 90.9 | 9.1 | 0.0
| MEX | 36.2 | 48.3 | 15.5
| MKK | 73.7 | 25.0 | 1.3
| TSI | 37.3 | 54.9 | 7.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23491141
|Title=Polymorphic variation within the ADAMTS2, ADAMTS14, ADAMTS5, ADAM12 and TIMP2 genes and the risk of Achilles tendon pathology: A genetic association study
}}

{{GET Evidence
|gene=ADAMTS2
|aa_change=Pro1177Ser
|aa_change_short=P1177S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1054480
|overall_frequency_n=2343
|overall_frequency_d=10756
|overall_frequency=0.217832
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=26
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.001
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}