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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)
Inborn genetic diseases
+5 more
GConflicting classifications of pathogenicity
NDE1, MYH11
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
NDE1, MYH11
Single nucleotide variant
(intron variant)
Stroke disorder
+2 more
GConflicting classifications of pathogenicity
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