NIBAN3
niban apoptosis regulator 3
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs754299971 | 19:17,634,260 | C/G | — | uncertain significance |
| rs1423310487 | 19:17,638,094 | G/A | — | uncertain significance |
| rs753211483 | 19:17,638,097 | C/T | — | uncertain significance |
| rs141221433 | 19:17,638,159 | C/T | — | uncertain significance |
| rs1437772826 | 19:17,638,182 | G/C | — | uncertain significance |
| rs1020451298 | 19:17,638,190 | G/A | — | likely benign |
| rs1568442550 | 19:17,641,582 | T/A | — | uncertain significance |
| rs769020357 | 19:17,641,596 | C/T | — | uncertain significance |
| rs140895055 | 19:17,641,645 | G/A | — | uncertain significance |
| rs376837341 | 19:17,643,097 | G/A | — | uncertain significance |
| rs536652149 | 19:17,643,117 | C/T | — | uncertain significance |
| rs758986033 | 19:17,643,132 | C/T | — | uncertain significance |
| rs2512750007 | 19:17,643,162 | G/A | — | uncertain significance |
| rs1351116694 | 19:17,643,172 | G/A | — | uncertain significance |
| rs201345901 | 19:17,644,466 | G/T | — | uncertain significance |
| rs148620566 | 19:17,648,265 | C/T | — | uncertain significance |
| rs985026826 | 19:17,648,311 | G/C | — | uncertain significance |
| rs770088926 | 19:17,650,048 | G/C | — | uncertain significance |
| rs754707320 | 19:17,650,192 | G/C | — | uncertain significance |
| rs1327226581 | 19:17,650,213 | C/T | — | uncertain significance |
| rs749500381 | 19:17,650,475 | C/A | — | uncertain significance |
| rs140392723 | 19:17,651,201 | C/T | — | uncertain significance |
| rs934921674 | 19:17,651,213 | G/T | — | uncertain significance |
| rs576013351 | 19:17,651,234 | G/T | — | uncertain significance |
| rs2075926759 | 19:17,651,281 | C/A | — | likely benign |
| rs772538485 | 19:17,651,284 | A/C | — | uncertain significance |
| rs150439084 | 19:17,651,357 | G/T | — | uncertain significance |
| rs1429286608 | 19:17,651,389 | G/C | — | uncertain significance |
| rs369452509 | 19:17,652,945 | G/C | — | uncertain significance |
| rs199734357 | 19:17,652,979 | C/T | — | uncertain significance |
| rs201431632 | 19:17,653,000 | G/A | — | uncertain significance |
| rs368873219 | 19:17,653,011 | C/T | — | uncertain significance |
| rs780503397 | 19:17,653,017 | C/T | — | uncertain significance |
| rs530918243 | 19:17,653,018 | G/A | — | likely benign |
| rs779409000 | 19:17,654,138 | G/A | — | uncertain significance |
| rs758503031 | 19:17,654,141 | G/A | — | uncertain significance |
| rs2075989392 | 19:17,654,142 | T/C | — | uncertain significance |
| rs2512807346 | 19:17,654,165 | G/T | — | uncertain significance |
| rs140048862 | 19:17,654,192 | T/C | — | uncertain significance |
| rs141937404 | 19:17,654,351 | G/A | — | uncertain significance |
| rs754036620 | 19:17,654,436 | A/G | — | uncertain significance |
| rs202088970 | 19:17,657,540 | G/T | — | uncertain significance |
| rs374460967 | 19:17,657,570 | G/A | — | uncertain significance |
| rs747856592 | 19:17,657,576 | C/T | — | uncertain significance |
| rs151074024 | 19:17,657,580 | G/T | — | uncertain significance |
| rs201125699 | 19:17,657,610 | A/G | — | benign |
| rs113687477 | 19:17,659,514 | C/T | intron variant | — |
| rs1967330 | 19:17,659,683 | C/A | — | — |
| rs1405645522 | 19:17,664,250 | C/T | — | uncertain significance |
| rs1307702899 | 19:17,664,262 | C/T | — | uncertain significance |
| rs371879832 | 19:17,664,263 | A/G | — | likely benign |
| rs745566221 | 19:17,664,286 | G/T | — | uncertain significance |
| rs200266618 | 19:17,664,325 | G/A | — | uncertain significance |
| rs2512860075 | 19:17,664,334 | C/A | — | uncertain significance |
| rs758219177 | 19:17,664,335 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.