Total variants with conflicting interpretations: 7
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000243. |
rs11466023 | 0.01590 |
NM_000243. |
rs11466024 | 0.01456 |
NM_000492. |
rs115545701 | 0.00350 |
NM_000169. |
rs148158093 | 0.00040 |
NM_000169. |
rs104894845 | 0.00039 |
NM_000091. |
rs190598500 | 0.00035 |
Single allele |