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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPM3
(V837M +12 more)
Single nucleotide variant
(missense variant)
TRPM3-related disorder
+6 more
GPathogenic/Likely pathogenic
TRIM37
(E12fs +1 more)
Microsatellite
(frameshift variant +2 more)
Mulibrey nanism syndrome
+1 more
GPathogenic