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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861897, MHRT
+1 more
(R1699Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
Dilated cardiomyopathy 1S
+2 more
GUncertain significance
MHRT, MYH7
(Q1541L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GUncertain significance
MYH7
(L620fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1S
GLikely pathogenic
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