PIWIL2
piwi like RNA-mediated gene silencing 2
Summary
PIWIL2 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003 [PubMed 12906857]).[supplied by OMIM, Mar 2008]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1350382156 | 8:22,136,928 | G/A | — | uncertain significance |
| rs201164295 | 8:22,136,990 | G/A | — | uncertain significance |
| rs1429056626 | 8:22,136,999 | C/A | — | uncertain significance |
| rs768235671 | 8:22,137,042 | G/C | — | uncertain significance |
| rs778321322 | 8:22,137,090 | C/T | — | uncertain significance |
| rs2131979750 | 8:22,138,642 | G/T | — | uncertain significance |
| rs370713888 | 8:22,138,661 | G/A | — | uncertain significance |
| rs755819581 | 8:22,138,911 | G/T | — | uncertain significance |
| rs746864369 | 8:22,138,931 | C/T | — | uncertain significance |
| rs142658978 | 8:22,138,932 | G/A | — | likely benign |
| rs1207635789 | 8:22,138,942 | G/C | — | uncertain significance |
| rs76659506 | 8:22,138,953 | C/G | missense variant | — |
| rs372692314 | 8:22,138,983 | C/T | — | uncertain significance |
| rs1349218667 | 8:22,138,991 | G/T | — | uncertain significance |
| rs770104998 | 8:22,139,000 | A/G | — | uncertain significance |
| rs752372698 | 8:22,140,549 | C/T | — | likely benign |
| rs181413985 | 8:22,140,573 | C/T | — | likely benign |
| rs937481204 | 8:22,140,647 | A/G | — | likely benign |
| rs202186373 | 8:22,140,657 | G/A | — | uncertain significance |
| rs2486418084 | 8:22,140,692 | C/T | — | uncertain significance |
| rs371325885 | 8:22,140,702 | C/G | — | uncertain significance |
| rs2486418250 | 8:22,140,711 | C/T | — | uncertain significance |
| rs201231729 | 8:22,140,720 | G/A | — | likely benign |
| rs755506555 | 8:22,140,734 | A/C | — | uncertain significance |
| rs141882601 | 8:22,145,062 | C/A | — | uncertain significance |
| rs778911127 | 8:22,145,136 | A/C | — | uncertain significance |
| rs139570286 | 8:22,146,113 | A/G | — | uncertain significance |
| rs182655883 | 8:22,146,132 | G/T | — | uncertain significance |
| rs781230890 | 8:22,146,134 | C/A | — | uncertain significance |
| rs145109389 | 8:22,147,438 | C/G | — | uncertain significance |
| rs2486495583 | 8:22,161,550 | C/G | — | uncertain significance |
| rs1831116161 | 8:22,161,575 | A/G | — | uncertain significance |
| rs2486495832 | 8:22,161,593 | T/C | — | uncertain significance |
| rs781236280 | 8:22,161,617 | A/G | — | uncertain significance |
| rs1831117930 | 8:22,161,622 | A/G | — | uncertain significance |
| rs749111384 | 8:22,161,626 | G/A | — | uncertain significance |
| rs199877180 | 8:22,161,634 | C/T | — | uncertain significance |
| rs370764248 | 8:22,162,304 | T/C | — | uncertain significance |
| rs2486503658 | 8:22,163,446 | A/G | — | uncertain significance |
| rs766175030 | 8:22,163,467 | C/T | — | uncertain significance |
| rs76268852 | 8:22,165,341 | C/G | intron variant | — |
| rs1563380268 | 8:22,165,515 | A/C | — | uncertain significance |
| rs576540467 | 8:22,165,537 | C/G | — | likely benign |
| rs529353152 | 8:22,165,552 | G/A | — | uncertain significance |
| rs141332968 | 8:22,165,563 | C/A | — | uncertain significance |
| rs772112294 | 8:22,165,564 | G/A | — | uncertain significance |
| rs777028397 | 8:22,165,578 | G/A | — | uncertain significance |
| rs139133214 | 8:22,167,475 | T/C | — | uncertain significance |
| rs756790734 | 8:22,167,484 | G/T | — | uncertain significance |
| rs140302382 | 8:22,168,668 | T/G | — | uncertain significance |
| rs766974842 | 8:22,168,694 | A/G | — | uncertain significance |
| rs147710731 | 8:22,168,728 | G/A | — | likely benign |
| rs759158586 | 8:22,168,785 | G/A | — | uncertain significance |
| rs1209909543 | 8:22,172,573 | C/T | — | uncertain significance |
| rs138911748 | 8:22,172,581 | C/T | — | uncertain significance |
| rs145656783 | 8:22,172,605 | C/T | — | uncertain significance |
| rs1382835135 | 8:22,172,634 | G/T | — | uncertain significance |
| rs368692793 | 8:22,173,804 | G/A | — | uncertain significance |
| rs149330096 | 8:22,173,809 | A/G | — | uncertain significance |
| rs369997928 | 8:22,175,705 | C/T | — | uncertain significance |
| rs763827827 | 8:22,175,714 | T/G | — | uncertain significance |
| rs374379247 | 8:22,175,726 | C/T | — | uncertain significance |
| rs147192548 | 8:22,210,532 | C/G | — | uncertain significance |
| rs1032619011 | 8:22,210,558 | T/G | — | uncertain significance |
| rs577597815 | 8:22,211,795 | A/G | — | uncertain significance |
| rs772432822 | 8:22,212,886 | G/A | — | uncertain significance |
| rs369979223 | 8:22,212,914 | G/A | — | uncertain significance |
| rs2486655982 | 8:22,212,980 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.