Showing 1 to 9 of 9 rows
See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2023-02-06
2.6
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2023-02-06
2.5
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2023-02-06
2.4
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2023-02-06
2.3
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2021-03-30
2.2
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2021-03-30
2.1
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Likely Pathogenic
Pendred syndrome2021-03-30
2.0
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Uncertain Significance
Pendred syndrome2021-02-11
1.1
-SLC26A4
View NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)
Uncertain Significance
Pendred syndrome2020-08-26
1.0
-SLC26A4
Showing 1 to 9 of 9 rows