Total variants with conflicting interpretations: 10
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_206933. |
rs111033282 | 0.00569 |
NM_005141. |
rs6054 | 0.00275 |
NM_021870. |
rs148685782 | 0.00222 |
NM_000552. |
rs61750604 | 0.00094 |
NM_000488. |
rs121909551 | 0.00092 |
NM_021870. |
rs138511699 | 0.00050 |
NM_006514. |
rs151090729 | 0.00047 |
NM_000552. |
rs149834874 | |
NM_201253. |
rs398124615 | |
Single allele |