Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000243. |
rs11466023 | 0.01590 |
NM_000243. |
rs11466024 | 0.01456 |
NM_000243. |
rs104895094 | 0.00506 |
NM_000492. |
rs115545701 | 0.00350 |
NM_000169. |
rs148158093 | 0.00040 |
NM_007255. |
rs200503833 | 0.00019 |
NM_001267550. |
rs747662439 | 0.00001 |
Single allele |