Total variants with conflicting interpretations: 5
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000410. |
rs1799945 | 0.10170 |
NM_001127701. |
rs17580 | 0.02950 |
NM_001127701. |
rs28929470 | 0.00211 |
NM_000463. |
rs35350960 | |
Single allele |