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Items: 3

  • The following term was not found in ClinVar: Trichoglottis.
Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(I521T)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance
MYH7
(R281T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GPathogenic/Likely pathogenic
MYH7
(R204L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+3 more
GPathogenic/Likely pathogenic
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