Total variants with conflicting interpretations: 5
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000314. |
rs1085308040 | |
NM_000314. |
rs398123316 | |
NM_000314. |
rs1085308047 | |
NM_000314. |
rs1085308056 | |
Single allele |