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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSHL1, GH-LCR
+1 more
Single nucleotide variant
(intron variant)
Ateleiotic dwarfism
+1 more
GConflicting classifications of pathogenicity
GH-LCR, SCN4A
(R1135P)
Single nucleotide variant
(missense variant)
Potassium-aggravated myotonia
GUncertain significance