SPAG7
sperm associated antigen 7
Summary
Predicted to enable nucleic acid binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants15 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768735296 | 17:4,862,840 | G/A | — | uncertain significance |
| rs768690755 | 17:4,863,145 | C/T | — | uncertain significance |
| rs1273912203 | 17:4,863,147 | C/T | — | uncertain significance |
| rs769767340 | 17:4,863,153 | G/C | — | uncertain significance |
| rs2507729233 | 17:4,863,333 | T/C | — | uncertain significance |
| rs201662286 | 17:4,863,367 | G/A | — | uncertain significance |
| rs238224 | 17:4,863,410 | G/A | — | benign |
| rs73343382 | 17:4,863,540 | T/C | — | benign |
| rs73343383 | 17:4,863,574 | G/A | — | benign |
| rs772163068 | 17:4,863,591 | C/G | — | uncertain significance |
| rs1446847296 | 17:4,863,814 | T/C | — | uncertain significance |
| rs369336761 | 17:4,864,136 | C/T | — | uncertain significance |
| rs182635218 | 17:4,864,137 | G/A | — | uncertain significance |
| rs747967498 | 17:4,871,068 | G/C | — | uncertain significance |
| rs149066790 | 17:4,871,572 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.