ZNHIT2
zinc finger HIT-type containing 2
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1046912 | 11:64,883,547 | G/A | downstream gene variant | — |
| rs200656382 | 11:64,883,958 | C/T | — | uncertain significance |
| rs752998089 | 11:64,884,002 | A/G | — | uncertain significance |
| rs755999355 | 11:64,884,018 | C/T | — | uncertain significance |
| rs2539168207 | 11:64,884,038 | C/G | — | uncertain significance |
| rs771277843 | 11:64,884,054 | C/T | — | uncertain significance |
| rs2539168316 | 11:64,884,090 | A/T | — | uncertain significance |
| rs374889298 | 11:64,884,105 | G/T | — | uncertain significance |
| rs1185226226 | 11:64,884,135 | C/A | — | uncertain significance |
| rs1007757155 | 11:64,884,170 | C/T | — | uncertain significance |
| rs759333110 | 11:64,884,275 | C/T | — | uncertain significance |
| rs2539168811 | 11:64,884,281 | C/G | — | uncertain significance |
| rs375144201 | 11:64,884,306 | C/T | — | uncertain significance |
| rs764005131 | 11:64,884,369 | C/A | — | uncertain significance |
| rs1222433065 | 11:64,884,393 | G/A | — | uncertain significance |
| rs372200131 | 11:64,884,444 | G/C | — | uncertain significance |
| rs1423877203 | 11:64,884,466 | G/T | — | uncertain significance |
| rs780921244 | 11:64,884,572 | G/A | — | uncertain significance |
| rs369408043 | 11:64,884,584 | A/G | — | uncertain significance |
| rs559096123 | 11:64,884,606 | G/C | — | uncertain significance |
| rs374326004 | 11:64,884,638 | G/A | — | uncertain significance |
| rs768133640 | 11:64,884,646 | C/A | — | uncertain significance |
| rs554302041 | 11:64,884,662 | T/C | — | uncertain significance |
| rs139901800 | 11:64,884,680 | C/T | — | uncertain significance |
| rs542986811 | 11:64,884,683 | C/G | — | uncertain significance |
| rs773795547 | 11:64,884,711 | G/A | — | uncertain significance |
| rs1038761996 | 11:64,884,729 | G/A | — | uncertain significance |
| rs200126440 | 11:64,884,755 | G/A | — | uncertain significance |
| rs759695398 | 11:64,884,810 | C/T | — | uncertain significance |
| rs2539170272 | 11:64,884,864 | A/G | — | likely benign |
| rs745901708 | 11:64,884,902 | C/A | — | uncertain significance |
| rs763219479 | 11:64,884,921 | G/A | — | uncertain significance |
| rs34563314 | 11:64,884,936 | G/A | — | benign |
| rs1948006371 | 11:64,884,945 | G/A | — | uncertain significance |
| rs1383381214 | 11:64,884,956 | C/A | — | uncertain significance |
| rs200891198 | 11:64,885,007 | G/A | — | uncertain significance |
| rs1001542660 | 11:64,885,032 | G/C | — | uncertain significance |
| rs1948008130 | 11:64,885,043 | G/A | — | uncertain significance |
| rs997645681 | 11:64,885,044 | G/A | — | uncertain significance |
| rs1948008241 | 11:64,885,047 | C/T | — | uncertain significance |
| rs34393594 | 11:64,885,102 | G/A | — | benign |
| rs1948009854 | 11:64,885,103 | C/G | — | uncertain significance |
| rs748350558 | 11:64,885,119 | G/C | — | uncertain significance |
| rs184963500 | 11:64,885,152 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.