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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLCN
(Q425R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
FLCN
(S331P +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
FLCN
(S79A)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+2 more
GUncertain significance
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