Total variants with conflicting interpretations: 9
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000410. |
rs1799945 | 0.10170 |
NM_000410. |
rs1800562 | 0.03880 |
NM_001127701. |
rs17580 | 0.02950 |
NM_019616. |
rs121964926 | 0.00118 |
NM_000463. |
rs34946978 | 0.00053 |
NM_000157. |
rs367968666 | 0.00016 |
NM_000155. |
rs111033640 | |
NM_000463. |
rs35350960 | |
Single allele |