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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(S1005L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
+3 more
GUncertain significance
FLNC, FLNC-AS1
(M2250L +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity