Total variants with conflicting interpretations: 15
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000277. |
rs1718301 | 0.37849 |
NM_000277. |
rs59326968 | 0.04425 |
NM_000277. |
rs62508624 | 0.02868 |
NM_000277. |
rs61747292 | 0.01582 |
NM_000277. |
rs142934616 | 0.00496 |
NM_000277. |
rs75065106 | 0.00272 |
NM_000277. |
rs118092776 | 0.00091 |
NM_000277. |
rs62508592 | 0.00087 |
NM_000277. |
rs145692106 | 0.00019 |
NM_000277. |
rs138355741 | 0.00008 |
NM_000277. |
rs62510582 | 0.00002 |
NM_000277. |
rs62514928 | 0.00001 |
NM_000277. |
rs77554925 | |
NM_000277. |
rs398123293 | |
Single allele |