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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT3
(R63C +7 more)
Single nucleotide variant
(missense variant +1 more)
Arthyrgryposis, distal, type 2B
+2 more
GPathogenic/Likely pathogenic
TNNT3
(R100H +8 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, distal, type 2B2
GUncertain significance