{{Rsnum
|rsid=10910078
|Chromosome=1
|position=2459149
|Orientation=plus
|GMAF=0.3352
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PLCH2
|Gene_s=PLCH2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 28.3 | 44.2 | 27.4
| HCB | 83.2 | 15.3 | 1.5
| JPT | 83.2 | 15.0 | 1.8
| YRI | 49.0 | 40.1 | 10.9
| ASW | 42.1 | 43.9 | 14.0
| CHB | 83.2 | 15.3 | 1.5
| CHD | 75.2 | 22.9 | 1.8
| GIH | 36.6 | 54.5 | 8.9
| LWK | 41.8 | 47.3 | 10.9
| MEX | 53.4 | 39.7 | 6.9
| MKK | 42.3 | 48.1 | 9.6
| TSI | 23.5 | 47.1 | 29.4
| HapMapRevision=28
}}{{PMID|22197933}} each copy of a T at [[rs10910078]] (equivalent to [[rs2477686]] in the study) was associated with about 1.4 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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}