Total variants with conflicting interpretations: 14
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_031407. |
rs140734968 | 0.00558 |
NM_031407. |
rs149893977 | 0.00142 |
NM_031407. |
rs145758265 | 0.00081 |
NM_031407. |
rs148129382 | 0.00050 |
NM_031407. |
rs142574684 | 0.00025 |
NM_031407. |
rs149577148 | 0.00024 |
NM_031407. |
rs1269602767 | 0.00007 |
NM_031407. |
rs149435515 | 0.00006 |
NM_031407. |
rs782526786 | 0.00004 |
NM_031407. |
rs782234241 | 0.00003 |
NM_031407. |
rs782009073 | 0.00001 |
NM_031407. |
rs1430366832 | 0.00001 |
NM_031407. |
rs1045935059 | 0.00001 |
Single allele | rs1556502214 |