Genetic Variant Clinical Significance (ClinVar). Genetic variant clinical significance from ClinVar by rsID, ClinVar id (VCV) or HGVS: pathogenic / benign / uncertain classification, review status with 0-4 stars, conditions, genes, molecular consequence, protein change and last evaluated date, best-reviewed record first. NCBI ClinVar, public domain; not medical advice.
| Network | Scheme | Amount | Pay To |
|---|---|---|---|
| solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp | exact | 0.00 tokens | 7LSjfr...acy7 |
| solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp | exact | 0.00 tokens | 7LSjfr...acy7 |
| Base | exact | $0.003000 USDC | 0xA2A8...c8aa |
| Polygon | exact | $0.003000 USDC | 0xA2A8...c8aa |
| Arbitrum One | exact | $0.003000 USDC | 0xA2A8...c8aa |
| solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp | exact | 0.02 tokens | 7LSjfr...acy7 |