{{Rsnum
|rsid=10498635
|Gene=RIN3
|Chromosome=14
|position=92636964
|Orientation=plus
|GMAF=0.09826
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RIN3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.0 | 18.6 | 4.4
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 87.8 | 11.6 | 0.7
| ASW | 89.5 | 10.5 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 78.2 | 18.8 | 3.0
| LWK | 83.6 | 15.5 | 0.9
| MEX | 84.5 | 15.5 | 0.0
| MKK | 82.7 | 15.4 | 1.9
| TSI | 64.7 | 31.4 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21623375
|Trait=None
|Title=Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
|RiskAllele=C
|Pval=3E-11
|OR=1.4400
|ORtxt=[1.29-1.60]
}}

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