Total variants with conflicting interpretations: 4
HGVS | dbSNP | gnomAD frequency |
---|---|---|
Single allele | rs114666055 | 0.00493 |
NM_012470. |
rs142359170 | 0.00093 |
NM_012470. |
rs61756249 | 0.00061 |
NM_012470. |
rs190759031 | 0.00005 |