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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNA
(H506P +2 more)
Single nucleotide variant
(missense variant)
not provided
+20 more
GUncertain significance
LMNA
(R541H +2 more)
Single nucleotide variant
(missense variant +1 more)
Hutchinson-Gilford syndrome
+7 more
GPathogenic/Likely pathogenic