Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000487. |
rs2071421 | 0.19530 |
NM_000036. |
rs17602729 | 0.08701 |
NM_000402. |
rs1050829 | 0.08672 |
NM_000041. |
rs7412 | 0.07986 |
NM_000155. |
rs2070074 | 0.07150 |
Single allele |