Total variants with conflicting interpretations: 11
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000535. |
rs121434629 | 0.00018 |
NM_000277. |
rs5030852 | 0.00004 |
NM_138694. |
rs148617572 | 0.00002 |
NM_000528. |
rs938576591 | 0.00001 |
NM_001360. |
rs779709646 | 0.00001 |
NM_001360. |
rs138659167 | |
NM_003309. |
rs775957625 | |
NM_006086. |
rs864321716 | |
NM_015338. |
rs750318549 | |
NM_078480. |
rs1057518681 | |
Single allele |