SYCP2L

synaptonemal complex protein 2 like

Summary

Predicted to act upstream of or within negative regulation of programmed cell death. Located in condensed chromosome, centromeric region and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants66 total

rsidPosition (GRCh37)AllelesClassClinVar
rs93798966:10,886,949C/Tregulatory region variant—
rs93487246:10,887,276C/Gregulatory region variant—
rs17801717316:10,891,758G/T—uncertain significance
rs3688394296:10,891,783G/A—uncertain significance
rs93666646:10,892,499T/Cintron variant—
rs7693350516:10,894,116C/T—likely benign
rs7548621186:10,894,388G/A—likely benign
rs21531576:10,897,488G/Aintron variant—
rs7583420156:10,898,259G/A—uncertain significance
rs3685830686:10,898,284C/T—likely benign
rs14492631726:10,903,118C/T—uncertain significance
rs3692300806:10,903,138G/A—uncertain significance
rs13540291686:10,903,184T/C—uncertain significance
rs3696874586:10,906,269A/G—uncertain significance
rs7623305836:10,907,805C/G—uncertain significance
rs7673435956:10,907,819A/G—uncertain significance
rs25328060236:10,907,871T/C—uncertain significance
rs7713121696:10,907,880A/C—uncertain significance
rs7729375966:10,910,390C/T—uncertain significance
rs14731566946:10,910,420G/C—uncertain significance
rs1898365276:10,912,986A/G—pathogenic
rs1997686346:10,912,993G/A—likely benign
rs3748541086:10,913,137C/T—uncertain significance
rs1909948066:10,921,531G/Aintron variant—
rs3719841976:10,924,740A/T—uncertain significance
rs25328337606:10,924,749T/C—likely benign
rs7765779556:10,927,474G/C—likely benign
rs7472964696:10,927,526C/T—uncertain significance
rs1480748066:10,927,527G/A—uncertain significance
rs1819554586:10,927,539C/G—uncertain significance
rs7476136556:10,927,540T/C—likely benign
rs9214403626:10,927,549A/C—uncertain significance
rs25328389986:10,927,595A/G—uncertain significance
rs14329439476:10,927,596G/A—uncertain significance
rs7722000296:10,928,661T/C—uncertain significance
rs2008240466:10,928,673C/T—uncertain significance
rs25328449316:10,930,642C/T—likely pathogenic
rs7757166296:10,931,697G/A—uncertain significance
rs122148256:10,933,378C/Tdownstream gene variant—
rs7736191486:10,935,330C/A—uncertain significance
rs3699267736:10,935,331A/G—uncertain significance
rs2009239436:10,935,412A/G—uncertain significance
rs5324688576:10,942,716G/A—uncertain significance
rs25328642826:10,942,728C/T—uncertain significance
rs10131337096:10,942,758C/T—uncertain significance
rs9150491726:10,942,911T/C—likely benign
rs7785336406:10,942,926C/T—uncertain significance
rs3718597716:10,942,934G/C—uncertain significance
rs2016426726:10,942,949A/G—uncertain significance
rs7697933116:10,942,959T/G—uncertain significance
rs728233496:10,950,047A/Tintron variant—
rs7688041956:10,955,351A/G—uncertain significance
rs1387597106:10,956,414A/T—uncertain significance
rs2004545206:10,956,416G/A—uncertain significance
rs7797308506:10,956,449A/G—uncertain significance
rs7585795906:10,956,467A/G—uncertain significance
rs7515931806:10,959,091C/G—uncertain significance
rs69189366:10,960,158G/Cintron variant—
rs69202476:10,960,173C/A——
rs17815936486:10,961,751T/A—uncertain significance
rs7644918146:10,964,032C/T—uncertain significance
rs94681266:10,966,541T/Aintron variant—
rs681487476:10,967,020A/G——
rs728233826:10,967,133G/T——
rs47131036:10,969,141G/A——
rs93685126:10,975,032C/Gdownstream gene variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.