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Items: 3

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr17:17119820-17119822
GRCh38:
Chr17:17216506-17216508
FLCNMultiple fibrofolliculomas, not specified, not provided,
Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Oct 24, 2016)
criteria provided, conflicting interpretations
2.
GRCh37:
Chr17:17118304
GRCh38:
Chr17:17214990
FLCNMultiple fibrofolliculomas, not providedPathogenic
(Jul 18, 2016)
criteria provided, multiple submitters, no conflicts
3.
FLCNPneumothorax, primary spontaneousPathogenic
(Apr 1, 2010)
no assertion criteria provided
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