Showing 1 to 3 of 3 rows
See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_004333.6(BRAF):c.622A>G (p.Ile208Val)
Likely Benign
RASopathy2022-08-23
2.1
-BRAF
View NM_004333.6(BRAF):c.622A>G (p.Ile208Val)
Likely Benign
RASopathy2022-08-11
2.0
-BRAF
View NM_004333.6(BRAF):c.622A>G (p.Ile208Val)
Uncertain Significance
RASopathy2020-03-09
1.0
-BRAF
Showing 1 to 3 of 3 rows