Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000535. |
rs587780057 | 0.00174 |
NM_000535. |
rs267608161 | 0.00003 |
NM_000535. |
rs587779338 | 0.00002 |
NM_000535. |
rs587779337 | 0.00001 |
NM_000535. |
rs587779335 | |
NM_000535. |
rs587780059 | |
NM_000535. |
rs786202098 | |
Single allele |