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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C2orf88, MSTN
(K153R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
MSTN, C2orf88
Single nucleotide variant
(intron variant)
Myostatin-related muscle hypertrophy
GPathogenic
C2orf88, MSTN
(A55T)
Single nucleotide variant
(missense variant)
MSTN-related condition
+1 more
GBenign
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