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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL41
(L145del)
Microsatellite
(inframe_deletion)
Nemaline myopathy 9
+1 more
GUncertain significance
KLHL41
Single nucleotide variant
(synonymous variant)
Nemaline myopathy 9
+2 more
GBenign/Likely benign