Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_002880. |
rs1057517887 | 0.00001 |
NM_002880. |
rs730880382 | |
NM_002880. |
||
NM_002880. |
rs1057524239 | |
NM_002880. |
||
NM_002880. |
rs397516821 | |
NM_002880. |
rs397516825 | |
Single allele |