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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNIP1, KCNMB1
(R140W)
Single nucleotide variant
(missense variant +1 more)
KCNMB1-related disorder
GBenign
KCNIP1, KCNMB1
Single nucleotide variant
(synonymous variant +1 more)
KCNMB1-related disorder
GLikely benign
KCNIP1, KCNMB1
(E65K)
Single nucleotide variant
(missense variant +1 more)
KCNMB1-related disorder
GBenign
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