{{Rsnum
|rsid=955988
|Chromosome=1
|position=106797973
|Orientation=plus
|GMAF=0.2172
|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 | 0.9 | 23.9 | 75.2
| HCB | 8.8 | 38.0 | 53.3
| JPT | 3.5 | 34.5 | 61.9
| YRI | 11.6 | 50.3 | 38.1
| ASW | 5.3 | 35.1 | 59.6
| CHB | 8.8 | 38.0 | 53.3
| CHD | 7.3 | 41.3 | 51.4
| GIH | 0.0 | 26.7 | 73.3
| LWK | 12.7 | 45.5 | 41.8
| MEX | 1.7 | 39.7 | 58.6
| MKK | 16.1 | 43.9 | 40.0
| TSI | 1.0 | 19.6 | 79.4
| HapMapRevision=28
}}{{PMID|22197933}} each copy of a C at [[rs955988]] (equivalent to [[rs12097821]] in the study) was associated with 1.25 times higher odds of non-obstructive azoospermia

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