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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMNA, LOC129931597
(R11C)
Single nucleotide variant
(missense variant +2 more)
Charcot-Marie-Tooth disease type 2
+2 more
GUncertain significance
LMNA, LOC129931597
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease type 2
+20 more
GBenign/Likely benign