rs2497600863
This variant is located in the SCN2B gene.
▶ClinVar annotation
About SCN2B
The protein encoded by this gene is the beta 2 subunit of the type II voltage-gated sodium channel. The encoded protein is involved in cell-cell adhesion and cell migration. Defects in this gene can be a cause of Brugada Syndrome, atrial fibrillation, or sudden infant death syndrome. [provided by RefSeq, Jul 2015]
View all SCN2B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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