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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN2B
Single nucleotide variant
(3 prime UTR variant)
Atrial fibrillation, familial, 14
GUncertain significance
SCN2B
(R185T)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 14
+1 more
GUncertain significance
SCN2B
(S29N)
Single nucleotide variant
(missense variant)
Atrial fibrillation, familial, 14
GUncertain significance
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