PRSS36
serine protease 36
Summary
Enables serine-type endopeptidase activity. Predicted to be involved in proteolysis. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs769045823 | 16:31,150,507 | C/A | — | likely benign |
| rs150721434 | 16:31,150,559 | G/C | — | uncertain significance |
| rs138987800 | 16:31,150,563 | G/A | — | uncertain significance |
| rs752642543 | 16:31,150,658 | C/G | — | uncertain significance |
| rs143567197 | 16:31,150,683 | C/T | — | uncertain significance |
| rs561297783 | 16:31,150,694 | G/T | — | uncertain significance |
| rs141363882 | 16:31,150,703 | G/A | — | uncertain significance |
| rs2544192726 | 16:31,150,709 | T/C | — | uncertain significance |
| rs560900074 | 16:31,151,640 | G/C | — | uncertain significance |
| rs1159309495 | 16:31,151,855 | C/A | — | uncertain significance |
| rs1031332082 | 16:31,151,915 | C/A | — | uncertain significance |
| rs368396607 | 16:31,151,917 | C/T | — | uncertain significance |
| rs533920941 | 16:31,151,918 | G/A | — | uncertain significance |
| rs746022666 | 16:31,151,947 | G/A | — | uncertain significance |
| rs371765050 | 16:31,151,975 | G/A | — | uncertain significance |
| rs768053646 | 16:31,151,992 | C/T | — | uncertain significance |
| rs1463655497 | 16:31,152,001 | T/A | — | uncertain significance |
| rs199965759 | 16:31,152,011 | G/C | — | uncertain significance |
| rs1294763356 | 16:31,152,019 | G/A | — | uncertain significance |
| rs753932010 | 16:31,152,022 | C/G | — | uncertain significance |
| rs773231251 | 16:31,152,851 | C/T | — | uncertain significance |
| rs951361732 | 16:31,152,853 | C/T | — | uncertain significance |
| rs145938370 | 16:31,152,873 | C/T | — | likely benign |
| rs1299806267 | 16:31,153,062 | G/C | — | uncertain significance |
| rs2057694854 | 16:31,153,064 | G/T | — | uncertain significance |
| rs1489713495 | 16:31,153,100 | C/T | — | uncertain significance |
| rs2544199075 | 16:31,153,130 | T/G | — | uncertain significance |
| rs148038859 | 16:31,153,136 | C/T | — | uncertain significance |
| rs1596845885 | 16:31,153,807 | A/C | — | uncertain significance |
| rs2057717055 | 16:31,153,817 | C/G | — | uncertain significance |
| rs1216216572 | 16:31,153,848 | G/T | — | uncertain significance |
| rs2057719952 | 16:31,153,873 | G/A | — | uncertain significance |
| rs751661423 | 16:31,153,899 | A/T | — | uncertain significance |
| rs1224195126 | 16:31,153,918 | C/T | — | uncertain significance |
| rs201556735 | 16:31,153,920 | C/T | — | uncertain significance |
| rs745365099 | 16:31,154,094 | C/T | — | uncertain significance |
| rs767571013 | 16:31,154,144 | G/C | — | uncertain significance |
| rs754664167 | 16:31,154,709 | G/T | — | uncertain significance |
| rs780649943 | 16:31,154,929 | T/C | — | uncertain significance |
| rs778876008 | 16:31,155,118 | C/T | — | uncertain significance |
| rs142392245 | 16:31,157,126 | C/T | — | uncertain significance |
| rs553867774 | 16:31,157,127 | G/A | — | uncertain significance |
| rs780293670 | 16:31,157,175 | T/C | — | uncertain significance |
| rs149468233 | 16:31,157,190 | C/T | — | uncertain significance |
| rs554980725 | 16:31,157,228 | A/C | — | uncertain significance |
| rs77284742 | 16:31,160,446 | C/T | — | uncertain significance |
| rs1382544542 | 16:31,160,490 | G/A | — | uncertain significance |
| rs2057856451 | 16:31,160,496 | G/T | — | uncertain significance |
| rs191779462 | 16:31,160,532 | G/T | missense variant | — |
| rs377306867 | 16:31,160,548 | G/A | — | uncertain significance |
| rs753032930 | 16:31,161,031 | G/T | — | uncertain significance |
| rs142912724 | 16:31,161,324 | C/T | — | likely benign |
| rs1173345850 | 16:31,161,325 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.