Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_003002. |
rs34677591 | 0.00706 |
NM_000169. |
rs149391489 | 0.00043 |
NM_000169. |
rs140329381 | 0.00009 |
NM_000527. |
rs138315511 | 0.00008 |
NM_000527. |
rs730882103 | 0.00002 |
Single allele |