CNBD2
cyclic nucleotide binding domain containing 2
Summary
Predicted to enable cAMP binding activity. Predicted to be involved in spermatogenesis. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs780350079 | 20:34,556,697 | A/T | — | uncertain significance |
| rs376975938 | 20:34,556,706 | T/C | — | likely benign |
| rs190908620 | 20:34,560,615 | G/T | — | uncertain significance |
| rs1356279893 | 20:34,560,624 | G/A | — | uncertain significance |
| rs6060732 | 20:34,561,480 | C/T | intron variant | — |
| rs55783707 | 20:34,563,384 | G/C | — | — |
| rs11908144 | 20:34,563,473 | T/A | — | — |
| rs780688317 | 20:34,563,880 | C/G | — | uncertain significance |
| rs138922540 | 20:34,563,887 | G/T | — | uncertain significance |
| rs765756199 | 20:34,568,408 | A/T | — | uncertain significance |
| rs184047696 | 20:34,568,423 | C/A | — | uncertain significance |
| rs745724867 | 20:34,568,456 | G/A | — | uncertain significance |
| rs201812279 | 20:34,568,489 | C/T | — | uncertain significance |
| rs372174146 | 20:34,568,498 | G/T | — | likely benign |
| rs373113225 | 20:34,568,535 | G/A | — | uncertain significance |
| rs200885142 | 20:34,571,911 | C/T | — | uncertain significance |
| rs138045142 | 20:34,571,912 | G/A | — | uncertain significance |
| rs144274307 | 20:34,571,918 | G/A | — | uncertain significance |
| rs746314671 | 20:34,571,945 | G/A | — | uncertain significance |
| rs551779036 | 20:34,572,029 | C/T | — | uncertain significance |
| rs750702259 | 20:34,572,591 | G/A | — | uncertain significance |
| rs957346583 | 20:34,572,598 | T/C | — | uncertain significance |
| rs147553424 | 20:34,572,627 | C/T | — | uncertain significance |
| rs201296527 | 20:34,572,668 | G/T | — | uncertain significance |
| rs1165541806 | 20:34,575,433 | C/A | — | uncertain significance |
| rs2516361914 | 20:34,575,443 | G/C | — | uncertain significance |
| rs34274439 | 20:34,582,976 | T/C | — | uncertain significance |
| rs745948902 | 20:34,583,045 | A/G | — | uncertain significance |
| rs367578003 | 20:34,583,069 | T/C | — | uncertain significance |
| rs529727580 | 20:34,589,426 | C/A | — | — |
| rs151123887 | 20:34,593,288 | G/A | intron variant | — |
| rs748383530 | 20:34,596,293 | C/T | — | uncertain significance |
| rs1023114031 | 20:34,596,314 | T/C | — | uncertain significance |
| rs2057013954 | 20:34,596,365 | A/G | — | uncertain significance |
| rs765026154 | 20:34,596,387 | C/T | — | uncertain significance |
| rs762828279 | 20:34,599,090 | A/G | — | uncertain significance |
| rs779254104 | 20:34,599,144 | G/A | — | likely benign |
| rs553984301 | 20:34,609,076 | C/T | — | — |
| rs6141590 | 20:34,610,256 | A/G | intron variant | — |
| rs200650618 | 20:34,611,546 | C/T | — | uncertain significance |
| rs147570074 | 20:34,611,581 | A/G | — | likely benign |
| rs144157412 | 20:34,611,602 | A/T | — | uncertain significance |
| rs1173806328 | 20:34,611,606 | G/T | — | uncertain significance |
| rs758063347 | 20:34,611,617 | G/A | — | uncertain significance |
| rs1436442355 | 20:34,611,623 | T/A | — | uncertain significance |
| rs552811368 | 20:34,611,678 | A/G | — | uncertain significance |
| rs2516514012 | 20:34,618,302 | T/G | — | uncertain significance |
| rs772511844 | 20:34,618,361 | C/A | — | uncertain significance |
| rs112300896 | 20:34,618,392 | G/A | — | likely benign |
| rs777056035 | 20:34,618,409 | A/G | — | uncertain significance |
| rs200247317 | 20:34,618,440 | T/C | — | uncertain significance |
| rs201193759 | 20:34,618,470 | G/A | — | uncertain significance |
| rs768966320 | 20:34,618,490 | C/A | — | uncertain significance |
| rs372470547 | 20:34,618,508 | C/A | — | uncertain significance |
| rs537703421 | 20:34,618,536 | C/G | — | uncertain significance |
| rs145803772 | 20:34,618,565 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.