{{Rsnum
|rsid=7302230
|Gene=CLSTN3
|Chromosome=12
|position=7135836
|Orientation=plus
|GMAF=0.02433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CLSTN3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 85.6 | 14.4 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 97.3 | 2.7 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 98.1 | 1.9 | 0.0
| MEX | 96.5 | 3.5 | 0.0
| MKK | 98.7 | 1.3 | 0.0
| TSI | 94.1 | 5.9 | 0.0
| HapMapRevision=28
}}According to a 2007 report, each G allele at [[rs7302230]] in the [[CLSTN3]] gene is associated with 1.6x higher odds of [[ankylosing spondylitis]]. {{PMID|17952073|OA=1
}}

{{GET Evidence
|gene=CLSTN3
|aa_change=Ser209Gly
|aa_change_short=S209G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7302230
|overall_frequency_n=479
|overall_frequency_d=10758
|overall_frequency=0.044525
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.003
|nblosum100=2
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}