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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH1
(A367T +1 more)
Single nucleotide variant
(missense variant)
Temple-Baraitser syndrome
+1 more
GUncertain significance
KCNH1
(R357Q +1 more)
Single nucleotide variant
(missense variant)
KCNH1-related disorders
+4 more
GPathogenic/Likely pathogenic