Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000252. |
rs781933660 | |
NM_000252. |
rs587783781 | |
NM_000252. |
rs587783783 | |
NM_000252. |
rs587783789 | |
NM_000252. |
rs587783796 | |
NM_000252. |
rs587783818 | |
NM_000252. |
rs587783842 | |
Single allele |