Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000243. |
rs11466023 | 0.01590 |
NM_000243. |
rs11466024 | 0.01456 |
NM_000287. |
rs34324426 | 0.00294 |
NM_001807. |
rs780419796 | 0.00115 |
NM_153676. |
rs146451547 | 0.00068 |
Single allele |