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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806427, TTN
(D12602N +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126806427, TTN
(R15103* +5 more)
Single nucleotide variant
(nonsense)
Primary dilated cardiomyopathy
+4 more
GPathogenic/Likely pathogenic
LOC126806427, TTN
(R12515Q +5 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
LOC126806427, TTN
(A13377E +5 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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