Total variants with conflicting interpretations: 9
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_001170629. |
rs1057524677 | |
NM_001170629. |
rs774906516 | |
NM_001170629. |
rs1555314911 | |
NM_001170629. |
rs1334692966 | |
NM_001170629. |
rs1555314211 | |
NM_001170629. |
rs1555314116 | |
NM_001170629. |
rs1085307794 | |
NM_001170629. |
rs1555318552 | |
Single allele |