EVA1C
eva-1 homolog C
Summary
Enables heparin binding activity. Located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs527851447 | 21:33,785,204 | C/T | — | uncertain significance |
| rs759104056 | 21:33,785,207 | G/A | — | uncertain significance |
| rs745868932 | 21:33,785,225 | C/T | — | uncertain significance |
| rs146014823 | 21:33,785,228 | C/A | — | likely benign |
| rs2033881667 | 21:33,785,235 | T/C | — | uncertain significance |
| rs1180391262 | 21:33,785,285 | T/G | — | uncertain significance |
| rs777470526 | 21:33,785,292 | A/T | — | uncertain significance |
| rs77135980 | 21:33,806,286 | C/G | — | — |
| rs35933282 | 21:33,808,520 | C/G | — | — |
| rs8134814 | 21:33,820,026 | G/A | — | — |
| rs2035656213 | 21:33,825,667 | G/C | — | uncertain significance |
| rs771280489 | 21:33,825,686 | A/G | — | uncertain significance |
| rs551596759 | 21:33,825,694 | C/T | — | uncertain significance |
| rs995885870 | 21:33,825,715 | C/G | — | uncertain significance |
| rs767344637 | 21:33,829,956 | A/T | — | uncertain significance |
| rs200043057 | 21:33,829,959 | C/T | — | uncertain significance |
| rs201176516 | 21:33,829,960 | G/A | — | uncertain significance |
| rs200325800 | 21:33,840,048 | C/G | — | uncertain significance |
| rs200288953 | 21:33,840,150 | C/A | — | uncertain significance |
| rs375945590 | 21:33,840,151 | C/G | — | uncertain significance |
| rs61739732 | 21:33,867,473 | C/T | — | benign |
| rs565328798 | 21:33,867,474 | G/T | — | uncertain significance |
| rs142626450 | 21:33,873,746 | C/T | — | uncertain significance |
| rs1363419373 | 21:33,876,244 | T/G | — | uncertain significance |
| rs751404995 | 21:33,876,319 | A/G | — | uncertain significance |
| rs59652870 | 21:33,882,403 | T/A | — | — |
| rs200503691 | 21:33,887,119 | T/C | — | benign |
| rs376116923 | 21:33,887,153 | G/A | — | uncertain significance |
| rs140738179 | 21:33,887,228 | C/A | — | uncertain significance |
| rs566223178 | 21:33,887,231 | G/A | — | uncertain significance |
| rs779127738 | 21:33,887,346 | C/G | — | uncertain significance |
| rs145086534 | 21:33,887,355 | G/A | — | uncertain significance |
| rs2517095413 | 21:33,887,389 | A/T | — | uncertain significance |
| rs61745002 | 21:33,887,483 | A/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.