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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNB2
(V115I +4 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+1 more
GUncertain significance
CACNB2
(A139S +4 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 4
+1 more
GUncertain significance
CACNB2
(M357L +9 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+1 more
GUncertain significance
CACNB2
(R473C +9 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 4
+1 more
GUncertain significance
CACNB2
(R568P +9 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 4
+2 more
GConflicting classifications of pathogenicity
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