Total variants with conflicting interpretations: 7
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000410. |
rs1800562 | 0.03880 |
NM_000055. |
rs1799807 | 0.01259 |
NM_005609. |
rs116315896 | 0.00530 |
NM_000350. |
rs1800553 | 0.00269 |
NM_000492. |
rs121908759 | 0.00039 |
NM_000261. |
rs74315339 | 0.00001 |
Single allele |