KCNK7
potassium two pore domain channel subfamily K member 7
Summary
This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel; however, it may require other non-pore-forming proteins for activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs369191636 | 11:65,360,547 | C/T | — | uncertain significance |
| rs376025958 | 11:65,360,571 | C/A | — | uncertain significance |
| rs201942855 | 11:65,360,606 | A/T | — | uncertain significance |
| rs758058773 | 11:65,360,636 | G/A | — | uncertain significance |
| rs146161072 | 11:65,360,956 | C/A | — | uncertain significance |
| rs779924861 | 11:65,361,001 | G/A | — | uncertain significance |
| rs749274421 | 11:65,361,004 | C/T | — | likely benign |
| rs148495696 | 11:65,361,063 | C/T | — | likely benign |
| rs745465268 | 11:65,361,165 | G/A | — | uncertain significance |
| rs752441429 | 11:65,361,210 | C/T | — | uncertain significance |
| rs1432330410 | 11:65,361,223 | G/A | — | uncertain significance |
| rs776803946 | 11:65,361,252 | G/A | — | uncertain significance |
| rs751500403 | 11:65,361,295 | C/A | — | uncertain significance |
| rs142989265 | 11:65,361,306 | G/A | — | uncertain significance |
| rs76353556 | 11:65,361,309 | T/C | — | benign |
| rs779357195 | 11:65,361,313 | C/T | — | uncertain significance |
| rs2496441745 | 11:65,361,316 | C/T | — | uncertain significance |
| rs76755084 | 11:65,361,338 | G/A | — | benign |
| rs752136574 | 11:65,362,949 | C/T | — | likely benign |
| rs770849577 | 11:65,363,101 | G/T | — | uncertain significance |
| rs747730582 | 11:65,363,228 | G/T | — | uncertain significance |
| rs72939147 | 11:65,364,335 | G/A | downstream gene variant | — |
| rs111669836 | 11:65,364,385 | T/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.