Total variants with conflicting interpretations: 17
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_006269. |
rs201493928 | 0.00005 |
NM_006269. |
rs180729424 | 0.00003 |
NM_006269. |
rs765129639 | 0.00002 |
NM_006269. |
rs1422250479 | 0.00001 |
NM_006269. |
rs750542962 | |
NM_006269. |
rs1365669334 | |
NM_006269. |
rs104894083 | |
NM_006269. |
rs755429480 | |
NM_006269. |
rs1585563283 | |
NM_006269. |
rs1554519555 | |
NM_006269. |
rs775731489 | |
NM_006269. |
rs1488237523 | |
NM_006269. |
||
NM_006269. |
rs797044735 | |
NM_006269. |
rs781249059 | |
NM_006269. |
rs1231321479 | |
Single allele |