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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FH
(Q108*)
Single nucleotide variant
(nonsense)
Hereditary leiomyomatosis and renal cell cancer
+3 more
GPathogenic/Likely pathogenic
PTCH1
(C37fs)
Deletion
(5 prime UTR variant +1 more)
Hereditary leiomyomatosis and renal cell cancer
+1 more
GUncertain significance