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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH11, NDE1
(E1833D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
MYH11, NDE1
Single nucleotide variant
(intron variant)
See cases
+3 more
GBenign/Likely benign
MYH11, NDE1
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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