Total variants with conflicting interpretations: 7
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_014336. |
rs1264794214 | 0.00001 |
NM_014336. |
rs201883601 | 0.00001 |
NM_014336. |
rs1597331616 | |
NM_014336. |
rs758001091 | |
NM_014336. |
rs1567637467 | |
NM_014336. |
rs751881283 | |
Single allele | rs1555547812 |