Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000363. |
rs727504243 | 0.00001 |
NM_000363. |
rs727504872 | |
NM_000363. |
rs397516351 | |
NM_000363. |
rs730881078 | |
NM_000363. |
rs730881083 | |
Single allele |