Total variants with conflicting interpretations: 17
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_031407. |
rs140734968 | 0.00558 |
NM_031407. |
rs149893977 | 0.00142 |
NM_031407. |
rs145758265 | 0.00081 |
NM_031407. |
rs142574684 | 0.00025 |
NM_031407. |
rs149435515 | 0.00006 |
NM_031407. |
rs782772316 | 0.00003 |
NM_031407. |
rs781928056 | 0.00002 |
NM_031407. |
rs782115290 | 0.00002 |
NM_031407. |
rs781931508 | 0.00002 |
NM_031407. |
rs782688724 | 0.00002 |
NM_031407. |
rs782428636 | 0.00002 |
NM_031407. |
rs782307186 | 0.00001 |
NM_031407. |
rs1012962799 | 0.00001 |
NM_031407. |
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NM_031407. |
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NM_031407. |
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Single allele | rs1556502223 |