Total variants with conflicting interpretations: 4
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000041. |
rs7412 | 0.07986 |
NM_000203. |
rs148775298 | 0.00274 |
NM_000520. |
rs121907970 | 0.00190 |
Single allele |