Total variants with conflicting interpretations: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_003000. |
rs33927012 | 0.00921 |
NM_144997. |
rs41419545 | 0.00217 |
NM_006015. |
rs113718290 | 0.00030 |
NM_000069. |
rs141204958 | 0.00029 |
NM_001943. |
rs576404380 | 0.00003 |
Single allele |