S I D E B A R
Format
Sort by

Download:

Choose Destination

Search results

Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr9:71650752
GRCh38:
Chr9:69035836
FXNFriedreich ataxia 1, not specified, Cardiovascular phenotype
Benign/Likely benign
(Jun 7, 2017)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr9:71661314
GRCh38:
Chr9:69046398
FXNnot specified, Cardiovascular phenotypeConflicting interpretations of pathogenicity
(Jan 31, 2017)
criteria provided, conflicting interpretations
Support Center