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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935183, TTN
+1 more
(A33673T +5 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
LOC129935183, TTN
+1 more
(E35299D +5 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1G
+5 more
GConflicting classifications of pathogenicity
LOC129935183, TTN
+1 more
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GConflicting classifications of pathogenicity
LOC129935183, TTN
+1 more
(A26198F +4 more)
Indel
(missense variant)
Cardiomyopathy
+8 more
GBenign/Likely benign
LOC129935183, TTN
+1 more
(A35263V +5 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+8 more
GBenign/Likely benign
LOC129935183, TTN
+1 more
(A35263S +5 more)
Single nucleotide variant
(missense variant)
not provided
+8 more
GBenign/Likely benign
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