CDHR2
cadherin related family member 2
Summary
This gene is a member of the protocadherin family, which represents a subset of the larger cadherin superfamily. The members of the protocadherin family encode non-classical cadherins that function as calcium-dependent cell-cell adhesion molecules. This protocadherin represents a new candidate for tumor suppression. Alternatively spliced transcript variants that encode the same protein have been identified. [provided by RefSeq, Jan 2010]
Known Variants94 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144863137 | 5:175,990,542 | C/T | intron variant | — |
| rs1171897795 | 5:175,992,691 | C/T | — | uncertain significance |
| rs750815475 | 5:175,992,712 | C/T | — | uncertain significance |
| rs1297038632 | 5:175,995,723 | C/T | — | uncertain significance |
| rs765026569 | 5:175,995,740 | G/T | — | likely benign |
| rs771363502 | 5:175,995,765 | G/A | — | likely benign |
| rs941027858 | 5:175,995,795 | C/G | — | uncertain significance |
| rs768142070 | 5:175,995,803 | C/T | — | likely benign |
| rs144430304 | 5:175,995,985 | A/G | — | uncertain significance |
| rs200376829 | 5:175,998,264 | C/T | — | likely benign |
| rs142176546 | 5:175,998,265 | G/A | — | uncertain significance |
| rs769314207 | 5:176,001,169 | A/T | — | uncertain significance |
| rs2532117410 | 5:176,002,323 | T/G | — | uncertain significance |
| rs565382865 | 5:176,002,399 | C/T | — | uncertain significance |
| rs374219258 | 5:176,002,523 | C/T | — | uncertain significance |
| rs144549731 | 5:176,002,580 | C/T | — | uncertain significance |
| rs374158863 | 5:176,002,731 | C/A | — | uncertain significance |
| rs1037173035 | 5:176,002,761 | A/T | — | uncertain significance |
| rs137860908 | 5:176,002,794 | G/C | — | uncertain significance |
| rs144535476 | 5:176,003,088 | G/A | — | uncertain significance |
| rs532896351 | 5:176,003,118 | G/A | — | uncertain significance |
| rs200775476 | 5:176,003,125 | A/T | — | uncertain significance |
| rs759818454 | 5:176,003,139 | C/G | — | uncertain significance |
| rs147274233 | 5:176,003,180 | G/A | — | likely benign |
| rs199841895 | 5:176,004,401 | G/A | — | uncertain significance |
| rs376960328 | 5:176,004,426 | G/A | — | likely benign |
| rs1479500830 | 5:176,004,472 | G/A | — | uncertain significance |
| rs34827556 | 5:176,004,490 | G/A | — | uncertain significance |
| rs915219569 | 5:176,004,502 | G/A | — | uncertain significance |
| rs764731410 | 5:176,004,639 | T/C | — | uncertain significance |
| rs200908807 | 5:176,004,723 | C/T | — | uncertain significance |
| rs767352630 | 5:176,004,739 | G/T | — | uncertain significance |
| rs115283964 | 5:176,004,743 | G/A | — | likely benign |
| rs374465389 | 5:176,004,788 | G/A | — | likely benign |
| rs756898008 | 5:176,005,056 | G/A | — | uncertain significance |
| rs374920977 | 5:176,005,079 | C/G | — | uncertain significance |
| rs776456392 | 5:176,005,090 | G/A | — | uncertain significance |
| rs1758451558 | 5:176,005,403 | G/C | — | uncertain significance |
| rs1176933386 | 5:176,005,407 | C/T | — | uncertain significance |
| rs200569396 | 5:176,005,443 | A/G | — | uncertain significance |
| rs114481367 | 5:176,005,517 | C/G | — | uncertain significance |
| rs753774305 | 5:176,005,568 | T/C | — | uncertain significance |
| rs575923102 | 5:176,008,426 | C/G | — | uncertain significance |
| rs2532129970 | 5:176,008,434 | C/A | — | uncertain significance |
| rs534536977 | 5:176,008,491 | G/A | — | uncertain significance |
| rs201340301 | 5:176,008,504 | G/A | — | uncertain significance |
| rs72809131 | 5:176,008,539 | G/A | — | likely benign |
| rs115353627 | 5:176,011,198 | A/G | — | likely benign |
| rs116786975 | 5:176,011,443 | G/A | — | uncertain significance |
| rs2532134409 | 5:176,011,476 | T/G | — | uncertain significance |
| rs377021257 | 5:176,011,548 | G/A | — | uncertain significance |
| rs143101284 | 5:176,011,558 | G/A | — | uncertain significance |
| rs1758608951 | 5:176,011,561 | T/C | — | uncertain significance |
| rs776550236 | 5:176,011,587 | G/A | — | uncertain significance |
| rs752765005 | 5:176,011,621 | C/G | — | uncertain significance |
| rs148792429 | 5:176,011,641 | G/T | — | uncertain significance |
| rs146363520 | 5:176,011,644 | G/T | — | uncertain significance |
| rs139706712 | 5:176,011,647 | G/A | — | uncertain significance |
| rs151175858 | 5:176,011,667 | C/T | — | likely benign |
| rs1439497935 | 5:176,011,692 | A/T | — | uncertain significance |
| rs199569019 | 5:176,011,731 | C/T | — | uncertain significance |
| rs766703295 | 5:176,011,783 | C/T | — | uncertain significance |
| rs774246443 | 5:176,011,834 | G/A | — | uncertain significance |
| rs201825073 | 5:176,011,912 | A/G | — | uncertain significance |
| rs2532135900 | 5:176,011,937 | G/T | — | uncertain significance |
| rs763466864 | 5:176,011,954 | C/T | — | uncertain significance |
| rs753338971 | 5:176,011,985 | G/A | — | likely benign |
| rs750406157 | 5:176,012,981 | G/A | — | uncertain significance |
| rs142234507 | 5:176,013,811 | G/A | — | uncertain significance |
| rs778289554 | 5:176,016,089 | G/C | — | uncertain significance |
| rs373435992 | 5:176,016,107 | G/C | — | uncertain significance |
| rs201059035 | 5:176,016,161 | G/A | — | likely benign |
| rs370718457 | 5:176,016,164 | G/A | — | uncertain significance |
| rs375103110 | 5:176,016,171 | C/T | — | uncertain significance |
| rs1758777881 | 5:176,016,407 | G/A | — | uncertain significance |
| rs761381922 | 5:176,016,560 | G/A | — | uncertain significance |
| rs202226659 | 5:176,017,452 | T/C | — | uncertain significance |
| rs2532146042 | 5:176,017,564 | G/C | — | uncertain significance |
| rs773380209 | 5:176,017,575 | G/C | — | uncertain significance |
| rs148287293 | 5:176,017,622 | G/C | — | uncertain significance |
| rs916329952 | 5:176,017,633 | G/A | — | uncertain significance |
| rs200440317 | 5:176,017,672 | G/A | — | likely benign |
| rs775076278 | 5:176,017,681 | C/T | — | uncertain significance |
| rs138471357 | 5:176,017,682 | G/A | — | uncertain significance |
| rs2532147031 | 5:176,018,216 | A/G | — | uncertain significance |
| rs751180171 | 5:176,018,219 | G/T | — | uncertain significance |
| rs890086618 | 5:176,018,224 | C/A | — | uncertain significance |
| rs754317963 | 5:176,018,248 | G/A | — | uncertain significance |
| rs966731069 | 5:176,018,473 | T/G | — | uncertain significance |
| rs752404135 | 5:176,019,725 | G/A | — | likely benign |
| rs1759005785 | 5:176,022,535 | G/C | — | uncertain significance |
| rs373675182 | 5:176,022,599 | C/T | — | uncertain significance |
| rs759135912 | 5:176,022,656 | G/C | — | uncertain significance |
| rs772890402 | 5:176,022,663 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.