Total variants with conflicting interpretations: 5
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000243. |
rs11466023 | 0.01590 |
NM_000518. |
rs33947415 | 0.00064 |
NM_000492. |
rs193922501 | 0.00003 |
NM_000143. |
rs587782207 | 0.00001 |
Single allele |