Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_001256317. |
rs56264519 | 0.00105 |
NM_000256. |
rs375882485 | 0.00010 |
NM_007126. |
rs121909334 | 0.00002 |
NM_000388. |
rs773146939 | 0.00001 |
NM_000166. |
rs863224471 | |
NM_000388. |
rs1576875819 | |
NM_003126. |
rs757679761 | |
Single allele |