ZNF91
zinc finger protein 91
Summary
The ZNF91 gene encodes a zinc finger protein of the KRAB (Kruppel-associated box) subfamily (Bellefroid et al., 1991, 1993 [PubMed 2023909] [PubMed 8467795]).[supplied by OMIM, May 2010]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs426564 | 19:23,497,013 | G/C | intron variant | — |
| rs295402 | 19:23,517,567 | A/C | — | — |
| rs7255761 | 19:23,528,353 | G/C | intron variant | — |
| rs374473001 | 19:23,542,272 | G/A | — | uncertain significance |
| rs760312253 | 19:23,542,285 | A/T | — | uncertain significance |
| rs1365880553 | 19:23,542,287 | A/C | — | uncertain significance |
| rs428549 | 19:23,542,290 | A/G | missense variant | — |
| rs1568381294 | 19:23,542,344 | G/A | — | uncertain significance |
| rs754567974 | 19:23,542,357 | C/A | — | uncertain significance |
| rs759136034 | 19:23,542,408 | T/C | — | uncertain significance |
| rs1432076401 | 19:23,542,434 | T/C | — | uncertain significance |
| rs2513196012 | 19:23,542,492 | T/C | — | uncertain significance |
| rs1968636945 | 19:23,542,500 | G/C | — | uncertain significance |
| rs202182741 | 19:23,542,632 | T/C | — | uncertain significance |
| rs768525091 | 19:23,542,648 | T/C | — | uncertain significance |
| rs1222136927 | 19:23,542,711 | A/G | — | uncertain significance |
| rs951089548 | 19:23,542,782 | C/T | — | uncertain significance |
| rs762775014 | 19:23,542,956 | T/G | — | uncertain significance |
| rs200697431 | 19:23,542,987 | G/C | — | uncertain significance |
| rs1045374145 | 19:23,543,046 | C/T | — | uncertain significance |
| rs906421826 | 19:23,543,050 | T/C | — | uncertain significance |
| rs755914444 | 19:23,543,140 | G/A | — | uncertain significance |
| rs146124770 | 19:23,543,172 | G/C | — | uncertain significance |
| rs201887473 | 19:23,543,206 | A/G | — | uncertain significance |
| rs1568383345 | 19:23,543,220 | T/A | — | uncertain significance |
| rs753790968 | 19:23,543,225 | T/G | — | uncertain significance |
| rs199921854 | 19:23,543,329 | T/C | — | uncertain significance |
| rs754217401 | 19:23,543,354 | A/T | — | likely benign |
| rs766458029 | 19:23,543,430 | G/A | — | uncertain significance |
| rs372751233 | 19:23,543,638 | T/C | — | uncertain significance |
| rs1968712420 | 19:23,543,650 | C/T | — | uncertain significance |
| rs769944057 | 19:23,543,667 | T/C | — | uncertain significance |
| rs553868508 | 19:23,543,691 | C/T | — | uncertain significance |
| rs778806756 | 19:23,543,749 | T/C | — | uncertain significance |
| rs2513201481 | 19:23,543,842 | T/C | — | uncertain significance |
| rs750976691 | 19:23,543,845 | C/T | — | uncertain significance |
| rs754723734 | 19:23,543,859 | T/C | — | uncertain significance |
| rs767650709 | 19:23,543,860 | G/A | — | uncertain significance |
| rs141572875 | 19:23,543,873 | G/A | — | likely benign |
| rs374679832 | 19:23,543,999 | T/C | — | uncertain significance |
| rs772530218 | 19:23,544,031 | T/G | — | uncertain significance |
| rs759045461 | 19:23,544,064 | G/A | — | uncertain significance |
| rs778896237 | 19:23,544,100 | G/A | — | uncertain significance |
| rs1299769165 | 19:23,544,129 | C/A | — | uncertain significance |
| rs1269137773 | 19:23,544,143 | G/C | — | uncertain significance |
| rs2513202942 | 19:23,544,207 | T/C | — | uncertain significance |
| rs568246653 | 19:23,544,246 | T/C | — | uncertain significance |
| rs1169679263 | 19:23,544,495 | G/A | — | uncertain significance |
| rs774630804 | 19:23,544,514 | T/G | — | uncertain significance |
| rs2145059231 | 19:23,544,588 | A/G | — | uncertain significance |
| rs745599269 | 19:23,544,660 | T/C | — | likely benign |
| rs1471381586 | 19:23,544,690 | G/A | — | uncertain significance |
| rs2513204737 | 19:23,544,696 | G/A | — | uncertain significance |
| rs763574074 | 19:23,544,728 | T/A | — | uncertain significance |
| rs780041403 | 19:23,544,759 | T/G | — | uncertain significance |
| rs759805313 | 19:23,544,793 | C/T | — | uncertain significance |
| rs200178015 | 19:23,544,858 | G/C | — | uncertain significance |
| rs1968825832 | 19:23,545,063 | A/G | — | uncertain significance |
| rs765077509 | 19:23,545,084 | T/G | — | uncertain significance |
| rs751528872 | 19:23,545,111 | T/C | — | uncertain significance |
| rs369764933 | 19:23,545,174 | C/T | — | uncertain significance |
| rs372804087 | 19:23,545,200 | C/T | — | uncertain significance |
| rs117266186 | 19:23,545,237 | G/A | — | likely benign |
| rs2513207024 | 19:23,545,264 | T/C | — | uncertain significance |
| rs760756933 | 19:23,545,354 | T/A | — | uncertain significance |
| rs375229716 | 19:23,545,404 | C/T | — | uncertain significance |
| rs368170174 | 19:23,545,407 | C/T | — | uncertain significance |
| rs778385594 | 19:23,545,467 | T/C | — | uncertain significance |
| rs148956643 | 19:23,556,550 | G/A | — | benign |
| rs369674549 | 19:23,556,559 | C/T | — | uncertain significance |
| rs377228317 | 19:23,556,604 | G/A | — | likely benign |
| rs34740519 | 19:23,556,605 | A/G | — | benign |
| rs760484360 | 19:23,557,538 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.