Total variants with conflicting interpretations: 11
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_002693. |
rs121918054 | 0.00096 |
NM_014053. |
rs556788423 | 0.00032 |
NM_000435. |
rs1167405466 | 0.00001 |
NM_000454. |
rs1424014997 | 0.00001 |
NM_000088. |
rs72645355 | |
NM_000435. |
rs886041513 | |
NM_000435. |
rs1064794216 | |
NM_004115. |
rs2035456443 | |
NM_014946. |
rs1553317025 | |
NM_033380. |
rs104886073 | |
Single allele |