Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_004562. |
rs771529549 | 0.00016 |
NM_004562. |
rs137853054 | 0.00016 |
NM_004562. |
rs191486604 | 0.00013 |
NM_004562. |
rs147757966 | 0.00006 |
NM_004562. |
rs137853060 | 0.00002 |
GRCh37/hg19 6q26 |