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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AARS2, POLR1C
(R199C)
Single nucleotide variant
(missense variant)
Combined oxidative phosphorylation defect type 8
+4 more
GPathogenic/Likely pathogenic
RYR1
(D4505H +1 more)
Single nucleotide variant
(missense variant)
Malignant hyperthermia, susceptibility to, 1
GBenign
RYR1
(P4905T +1 more)
Single nucleotide variant
(missense variant)
Congenital hip dislocation
+3 more
GUncertain significance
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