PHTF2
putative homeodomain transcription factor 2
Summary
Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs41281019 | 7:77,427,588 | C/A | regulatory region variant | — |
| rs10249075 | 7:77,452,430 | C/A | — | — |
| rs55759218 | 7:77,453,357 | G/C | — | — |
| rs1795766643 | 7:77,469,577 | C/T | — | uncertain significance |
| rs778356622 | 7:77,469,597 | A/G | — | uncertain significance |
| rs62462680 | 7:77,488,434 | A/T | intron variant | — |
| rs10272350 | 7:77,491,389 | G/A | intron variant | — |
| rs6465867 | 7:77,497,472 | T/C | intron variant | — |
| rs7786368 | 7:77,500,734 | T/C | intron variant | — |
| rs62462688 | 7:77,515,422 | A/G | — | — |
| rs73138439 | 7:77,516,344 | C/A | intron variant | — |
| rs202166525 | 7:77,522,948 | A/G | — | uncertain significance |
| rs2471604 | 7:77,525,387 | A/C | downstream gene variant | — |
| rs534841738 | 7:77,531,171 | C/T | — | uncertain significance |
| rs751697457 | 7:77,531,183 | C/G | — | uncertain significance |
| rs1437956156 | 7:77,538,124 | T/G | — | uncertain significance |
| rs2547157492 | 7:77,538,247 | C/T | — | uncertain significance |
| rs2547163802 | 7:77,539,575 | G/A | — | uncertain significance |
| rs375131045 | 7:77,539,632 | C/A | — | uncertain significance |
| rs61998250 | 7:77,539,677 | G/A | — | uncertain significance |
| rs933956162 | 7:77,539,689 | T/G | — | uncertain significance |
| rs906892872 | 7:77,549,660 | G/A | — | uncertain significance |
| rs375949234 | 7:77,549,684 | G/A | — | likely benign |
| rs368157181 | 7:77,549,730 | G/A | — | likely benign |
| rs12234571 | 7:77,549,906 | T/G | intron variant | — |
| rs372691512 | 7:77,552,022 | A/G | — | uncertain significance |
| rs559299935 | 7:77,552,037 | C/G | — | uncertain significance |
| rs369408811 | 7:77,552,048 | C/T | — | uncertain significance |
| rs752955673 | 7:77,552,070 | A/G | — | uncertain significance |
| rs1442642264 | 7:77,552,082 | A/G | — | uncertain significance |
| rs749115591 | 7:77,558,454 | G/C | — | uncertain significance |
| rs1214945595 | 7:77,558,469 | G/A | — | uncertain significance |
| rs2547226358 | 7:77,558,472 | C/G | — | uncertain significance |
| rs1460106309 | 7:77,558,570 | A/G | — | uncertain significance |
| rs199506255 | 7:77,558,607 | G/C | — | uncertain significance |
| rs2428940 | 7:77,564,448 | A/T | — | — |
| rs2547250008 | 7:77,567,085 | T/C | — | uncertain significance |
| rs762657549 | 7:77,569,351 | A/G | — | uncertain significance |
| rs1421985329 | 7:77,569,381 | T/A | — | uncertain significance |
| rs2547255872 | 7:77,569,462 | T/C | — | uncertain significance |
| rs1317437776 | 7:77,569,557 | C/T | — | uncertain significance |
| rs1386779216 | 7:77,569,906 | A/T | — | uncertain significance |
| rs848445 | 7:77,572,461 | T/C | intron variant | — |
| rs848446 | 7:77,573,156 | A/G | intron variant | — |
| rs117395201 | 7:77,574,637 | A/C | regulatory region variant | — |
| rs753986766 | 7:77,579,009 | C/G | — | uncertain significance |
| rs117514950 | 7:77,579,025 | T/A | — | uncertain significance |
| rs1291616039 | 7:77,580,988 | C/A | — | uncertain significance |
| rs759471348 | 7:77,583,129 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.