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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861897, MYH7
(A1763T)
Single nucleotide variant
(missense variant)
Myosin storage myopathy
+11 more
GUncertain significance
LOC126861897, MHRT
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Cardiomyopathy
GBenign
LOC126861897, MHRT
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
MYH7-related condition
+13 more
GBenign/Likely benign
LOC126861897, MHRT
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Cardiomyopathy
GBenign
LOC126861897, MHRT
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
LOC126861897, MHRT
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
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