Total variants with conflicting interpretations: 5
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_006846. |
rs142558269 | 0.00581 |
NM_006846. |
rs142227576 | 0.00313 |
NM_006846. |
rs181639116 | 0.00297 |
NM_006846. |
rs554634510 | |
Single allele |