BTBD7
BTB domain containing 7
Summary
Predicted to be involved in regulation of branching involved in salivary gland morphogenesis. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1595280098 | 14:93,708,736 | A/C | — | uncertain significance |
| rs775432782 | 14:93,708,739 | G/T | — | uncertain significance |
| rs200447121 | 14:93,708,756 | C/T | — | likely benign |
| rs1368651061 | 14:93,708,792 | A/G | — | uncertain significance |
| rs202055956 | 14:93,708,810 | G/A | — | likely benign |
| rs747016085 | 14:93,708,833 | G/C | — | uncertain significance |
| rs61740740 | 14:93,708,911 | C/T | — | uncertain significance |
| rs201912928 | 14:93,708,942 | G/A | — | uncertain significance |
| rs2505085703 | 14:93,708,971 | T/C | — | uncertain significance |
| rs751931563 | 14:93,708,976 | G/T | — | uncertain significance |
| rs147201730 | 14:93,709,071 | C/G | — | uncertain significance |
| rs200704553 | 14:93,709,094 | G/A | — | uncertain significance |
| rs745533607 | 14:93,709,136 | C/A | — | uncertain significance |
| rs1461316661 | 14:93,709,158 | T/C | — | uncertain significance |
| rs200000140 | 14:93,709,170 | T/C | — | uncertain significance |
| rs760882700 | 14:93,709,174 | G/T | — | uncertain significance |
| rs745694971 | 14:93,709,247 | C/T | — | uncertain significance |
| rs569825061 | 14:93,709,280 | G/A | — | uncertain significance |
| rs766575838 | 14:93,709,311 | C/G | — | uncertain significance |
| rs2052253571 | 14:93,709,356 | G/A | — | uncertain significance |
| rs370370251 | 14:93,709,395 | C/T | — | uncertain significance |
| rs183380362 | 14:93,709,433 | C/T | — | uncertain significance |
| rs746305889 | 14:93,712,223 | G/A | — | uncertain significance |
| rs962707312 | 14:93,712,271 | G/A | — | uncertain significance |
| rs143877217 | 14:93,712,317 | G/A | — | uncertain significance |
| rs372008556 | 14:93,712,362 | T/C | — | uncertain significance |
| rs2505109371 | 14:93,712,432 | G/T | — | uncertain significance |
| rs146941671 | 14:93,712,565 | G/A | — | uncertain significance |
| rs1260554040 | 14:93,712,568 | T/A | — | uncertain significance |
| rs201243121 | 14:93,714,886 | T/C | — | uncertain significance |
| rs200351621 | 14:93,714,943 | G/A | — | uncertain significance |
| rs370542488 | 14:93,714,950 | G/A | — | uncertain significance |
| rs150103724 | 14:93,714,994 | C/T | — | uncertain significance |
| rs374714816 | 14:93,717,896 | C/T | — | uncertain significance |
| rs2052368770 | 14:93,717,962 | G/A | — | uncertain significance |
| rs368923940 | 14:93,720,031 | G/A | — | uncertain significance |
| rs762370810 | 14:93,720,058 | G/A | — | uncertain significance |
| rs1049857465 | 14:93,720,091 | T/C | — | uncertain significance |
| rs2505165835 | 14:93,723,557 | T/C | — | uncertain significance |
| rs377109750 | 14:93,723,644 | C/T | — | uncertain significance |
| rs759891874 | 14:93,723,686 | C/T | — | uncertain significance |
| rs561482029 | 14:93,724,933 | T/A | — | — |
| rs374004567 | 14:93,727,967 | C/A | — | uncertain significance |
| rs1249318625 | 14:93,727,968 | A/G | — | uncertain significance |
| rs202129419 | 14:93,760,287 | C/T | — | uncertain significance |
| rs61747488 | 14:93,760,291 | C/A | — | uncertain significance |
| rs530220385 | 14:93,760,294 | C/T | — | uncertain significance |
| rs777385863 | 14:93,760,618 | C/T | — | uncertain significance |
| rs769964438 | 14:93,760,636 | T/G | — | uncertain significance |
| rs2547667635 | 14:93,760,655 | C/T | — | uncertain significance |
| rs2547667707 | 14:93,760,700 | C/A | — | uncertain significance |
| rs746181747 | 14:93,760,735 | C/T | — | uncertain significance |
| rs780728207 | 14:93,760,894 | C/T | — | uncertain significance |
| rs2547668172 | 14:93,760,936 | C/T | — | uncertain significance |
| rs751202083 | 14:93,760,978 | T/C | — | uncertain significance |
| rs200455654 | 14:93,761,256 | T/C | — | uncertain significance |
| rs2547668929 | 14:93,761,266 | G/C | — | uncertain significance |
| rs2273638 | 14:93,761,913 | A/G | intron variant | — |
| rs1180609332 | 14:93,762,329 | T/G | — | uncertain significance |
| rs756126969 | 14:93,762,363 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.