STPG2
sperm tail PG-rich repeat containing 2
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143475242 | 4:98,373,818 | C/T | intron variant | — |
| rs952714360 | 4:98,480,232 | C/T | — | likely benign |
| rs139805225 | 4:98,480,255 | T/C | — | uncertain significance |
| rs143881716 | 4:98,596,850 | G/T | — | — |
| rs150068765 | 4:98,633,897 | G/A | — | uncertain significance |
| rs138328166 | 4:98,762,004 | C/T | — | uncertain significance |
| rs759189218 | 4:98,762,007 | G/A | — | uncertain significance |
| rs546161121 | 4:98,800,392 | C/A | — | — |
| rs762768245 | 4:98,865,049 | A/G | — | uncertain significance |
| rs368781633 | 4:98,865,097 | T/C | — | uncertain significance |
| rs757544801 | 4:98,865,098 | A/G | — | uncertain significance |
| rs1215694639 | 4:98,865,139 | C/T | — | uncertain significance |
| rs201716501 | 4:98,893,451 | G/C | — | uncertain significance |
| rs2530139024 | 4:98,893,472 | G/T | — | uncertain significance |
| rs137988195 | 4:98,893,477 | G/A | — | likely benign |
| rs199644011 | 4:98,893,490 | G/A | — | uncertain significance |
| rs774870889 | 4:98,893,536 | G/C | — | uncertain significance |
| rs201860057 | 4:98,902,345 | C/T | — | uncertain significance |
| rs199854534 | 4:98,902,367 | G/T | — | uncertain significance |
| rs750242856 | 4:98,902,409 | C/T | — | uncertain significance |
| rs150708038 | 4:98,902,414 | C/T | — | uncertain significance |
| rs201834612 | 4:98,902,415 | G/C | — | uncertain significance |
| rs139988382 | 4:98,902,441 | G/A | — | uncertain significance |
| rs1727284 | 4:98,979,582 | C/G | — | — |
| rs140974931 | 4:98,984,061 | T/A | intron variant | — |
| rs761732035 | 4:99,027,112 | T/C | — | likely benign |
| rs755340295 | 4:99,027,185 | G/A | — | likely benign |
| rs199930977 | 4:99,030,413 | C/T | — | uncertain significance |
| rs372964222 | 4:99,049,602 | G/T | — | uncertain significance |
| rs765705550 | 4:99,049,622 | G/C | — | uncertain significance |
| rs1321918151 | 4:99,049,628 | G/A | — | uncertain significance |
| rs2530574857 | 4:99,049,636 | T/G | — | uncertain significance |
| rs529954852 | 4:99,049,695 | T/C | — | uncertain significance |
| rs776906107 | 4:99,055,581 | C/T | — | uncertain significance |
| rs371275654 | 4:99,064,249 | T/G | — | uncertain significance |
| rs144452195 | 4:99,064,252 | G/C | — | uncertain significance |
| rs747525997 | 4:99,064,273 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.