ADAMTS20

ADAM metallopeptidase with thrombospondin type 1 motif 20

Summary

The protein encoded by this gene is a member of the ADAMTS family of zinc-dependent proteases. The encoded protein has a signal peptide that is cleaved to release the mature peptide, which is secreted and found in the extracellular matrix. This protein may be involved in tissue remodeling. [provided by RefSeq, Sep 2011]

Known Variants111 total

rsidPosition (GRCh37)AllelesClassClinVar
rs36759053212:43,750,349A/Cuncertain significance
rs249856436412:43,763,147A/Clikely benign
rs78054462312:43,769,185T/Cuncertain significance
rs76132702212:43,769,251C/Guncertain significance
rs74788233612:43,769,866C/Tuncertain significance
rs19980199812:43,769,921G/Cuncertain significance
rs14912599412:43,770,133C/Tuncertain significance
rs76803693712:43,770,354C/Auncertain significance
rs249858764912:43,770,404G/Tuncertain significance
rs77959035212:43,770,422C/Guncertain significance
rs13875018212:43,770,437A/Guncertain significance
rs37527629712:43,771,248C/Tuncertain significance
rs14547429312:43,771,315G/Alikely benign
rs54241421312:43,771,326T/Cuncertain significance
rs37433657212:43,777,386A/Guncertain significance
rs249860775012:43,777,393T/Guncertain significance
rs13841332512:43,777,426G/Cuncertain significance
rs77795628512:43,777,494C/Tlikely benign
rs76440951212:43,777,642C/Tuncertain significance
rs75487882912:43,777,680C/Tuncertain significance
rs77031789012:43,777,762A/Guncertain significance
rs213725195712:43,792,961C/Auncertain significance
rs77337608412:43,792,987A/Guncertain significance
rs1078543012:43,819,298G/C
rs15106245812:43,819,318G/Auncertain significance
rs76279690512:43,819,379T/Clikely benign
rs74732908112:43,819,382C/Tuncertain significance
rs77003603212:43,819,388G/Auncertain significance
rs78149845712:43,819,481A/Guncertain significance
rs37741613812:43,821,148C/Tuncertain significance
rs78134198912:43,821,162C/Auncertain significance
rs77703871912:43,822,049C/Tuncertain significance
rs249829584112:43,822,052A/Guncertain significance
rs77042673412:43,822,263A/Cuncertain significance
rs77593742612:43,822,264T/Auncertain significance
rs14261552212:43,822,279T/Cuncertain significance
rs14678974312:43,822,485C/Auncertain significance
rs37637366012:43,822,565T/Cuncertain significance
rs76280944012:43,822,569G/Auncertain significance
rs141396110612:43,823,424G/Auncertain significance
rs76034013212:43,823,434C/Auncertain significance
rs74590461612:43,823,482C/Tlikely benign
rs13857328312:43,825,166C/Tuncertain significance
rs249830914512:43,825,247A/Guncertain significance
rs77736953412:43,825,265C/Tuncertain significance
rs11139606312:43,826,110G/Alikely benign
rs36829014212:43,826,130A/Cuncertain significance
rs36910150312:43,826,205G/Auncertain significance
rs76364293312:43,826,222A/Tuncertain significance
rs14156233312:43,826,248C/Tbenign
rs146647858212:43,826,249C/Tuncertain significance
rs76570799912:43,826,513G/Tuncertain significance
rs37393723112:43,826,524A/Cuncertain significance
rs18529513112:43,826,574C/Tuncertain significance
rs3604615612:43,826,590T/Abenign
rs77501337512:43,828,078G/Auncertain significance
rs76463409312:43,828,103G/Tuncertain significance
rs14633110212:43,828,117T/Guncertain significance
rs37362392612:43,833,432C/Tuncertain significance
rs14869689412:43,833,518G/Tuncertain significance
rs37203006512:43,833,527G/Cuncertain significance
rs249833589512:43,833,541C/Auncertain significance
rs74821125912:43,837,636G/Auncertain significance
rs249835021312:43,837,642C/Tuncertain significance
rs249835896812:43,840,454C/Guncertain significance
rs77454647012:43,846,160A/Tuncertain significance
rs249837681712:43,846,343A/Tuncertain significance
rs76052068912:43,846,379C/Tuncertain significance
rs77848457412:43,846,410A/Guncertain significance
rs156555539712:43,846,428G/Auncertain significance
rs14187911712:43,847,725C/Alikely benign
rs249838174712:43,847,756A/Cuncertain significance
rs140768408012:43,847,767C/Tuncertain significance
rs37083554412:43,847,780G/Cuncertain significance
rs249838199812:43,847,803T/Cuncertain significance
rs76943644012:43,847,813G/Auncertain significance
rs77544863412:43,847,821G/Alikely benign
rs77711576512:43,856,790G/Auncertain significance
rs54190659012:43,858,395A/Cuncertain significance
rs99369093612:43,858,443T/Cuncertain significance
rs75951166612:43,858,464C/Guncertain significance
rs13900599212:43,858,504G/Tuncertain significance
rs135115513312:43,860,509A/Glikely benign
rs249841135612:43,860,522A/Glikely benign
rs14959180212:43,860,531C/Tuncertain significance
rs75493817312:43,886,344T/Cuncertain significance
rs133547556812:43,887,014G/Tlikely benign
rs20118323912:43,887,056C/Guncertain significance
rs75473175312:43,895,962A/Guncertain significance
rs77658833112:43,896,046C/Auncertain significance
rs14550632312:43,896,064C/Auncertain significance
rs14883238612:43,896,065G/Auncertain significance
rs74773840112:43,896,165G/Tlikely benign
rs249849597712:43,896,190G/Auncertain significance
rs14585914912:43,925,854A/Guncertain significance
rs20130828112:43,925,865T/Guncertain significance
rs75558781912:43,925,904T/Auncertain significance
rs76596204512:43,925,952A/Tuncertain significance
rs129727857212:43,925,971C/Tuncertain significance
rs14104352912:43,925,997G/Alikely benign

Showing 100 of 111 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.