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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASTN2, TRIM32
Single nucleotide variant
(synonymous variant +1 more)
Sarcotubular myopathy
+3 more
GConflicting classifications of pathogenicity
ASTN2, TRIM32
Single nucleotide variant
(synonymous variant +1 more)
Bardet-Biedl syndrome
GLikely benign