Total variants with conflicting interpretations: 7
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000463. |
rs35003977 | 0.00034 |
NM_000508. |
rs121909608 | 0.00001 |
NM_000508. |
rs121909605 | 0.00001 |
NM_000402. |
rs387906468 | |
NM_000402. |
rs137852326 | |
NM_005141. |
rs121909616 | |
Single allele |