Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000444. |
rs886041446 | |
NM_000444. |
rs886041224 | |
NM_000444. |
rs1927568587 | |
NM_000444. |
rs1057520344 | |
NM_000444. |
rs866429868 | |
Single allele |