Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_002386. |
rs1805009 | 0.01121 |
NM_006214. |
rs62619919 | 0.00690 |
NM_001377. |
rs368802969 | 0.00476 |
NM_024072. |
rs148961522 | 0.00241 |
NM_018718. |
rs143303575 | 0.00218 |
Single allele |