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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806430, TTN
(I5054T +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
LOC126806430, TTN
(C5017S +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126806430, TTN
(A5867T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
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