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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNMA1, KCNMA1-AS1
(R1041C +9 more)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
KCNMA1, KCNMA1-AS1
(T943I +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance