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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARMC9
Single nucleotide variant
(splice acceptor variant)
not provided
+1 more
GLikely pathogenic
ARMC9
(R343C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
ARMC9
(P414L +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
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