Total variants with conflicting interpretations: 5
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000202. |
rs61736892 | 0.01492 |
NM_006950. |
rs200533370 | 0.01462 |
NM_000489. |
rs45439799 | 0.00663 |
NM_015141. |
rs72552293 | 0.00291 |
Single allele |