Total variants with conflicting interpretations: 4
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_001377. |
rs137853027 | 0.00026 |
NM_001377. |
rs368631447 | 0.00003 |
NM_002693. |
rs121918056 | 0.00001 |
Single allele |