Gene entry
SPATA16
spermatogenesis associated 16
- Chromosome
- 3
- Cytoband
- 3q26.31
- Variants (rsID)
- 51
SPATA16 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q26.31). Its official name is “spermatogenesis associated 16”. The reference table lists 51 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1515441Benignsingle nucleotide variantGlobozoospermia
- rs55724801Benignsingle nucleotide variantGlobozoospermia
- rs137853118Conflicting interpretationssingle nucleotide variantGlobozoospermia
- rs115095786Likely benignsingle nucleotide variantGlobozoospermia
Other listed variants
- rs484212
- rs575511
- rs1319176
- rs1353868
- rs1399750
- rs1515438
- rs2861071
- rs6445091
- rs6778909
- rs6781018
- rs7638139
- rs7645546
- rs9848803
- rs9851618
- rs10460879
- rs10460880
- rs11708501
- rs11720607
- rs13070200
- rs16846259
- rs16846428
- rs16846634
- rs17760014
- rs17828598
- rs34939098
- rs55768751
- rs67456152
- rs73175089
- rs73175098
- rs74610143
- rs75032014
- rs76845172
- rs77035727
- rs79132578
- rs79775469
- rs79908900
- rs113174271
- rs114974834
- rs115764681
- rs116438867
- rs116466451
- rs141845742
- rs149111804
- rs150581488
- rs185789602
- rs199868908
- rs202106536
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
