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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH2
(K557T +1 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 2
+7 more
GBenign
KCNH2
Single nucleotide variant
(synonymous variant +1 more)
Long QT syndrome
+5 more
GBenign
KCNH2
(R582C +4 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GPathogenic/Likely pathogenic
KCNH2
Single nucleotide variant
(synonymous variant +1 more)
Cardiac arrhythmia
+4 more
GBenign/Likely benign
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