ClinVar Miner

List of variants in gene SCN2B reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_004588.5(SCN2B):c.449-12C>A rs8192613 0.45401
NM_004588.5(SCN2B):c.498C>T (p.Val166=) rs200709238 0.00039
NM_004588.5(SCN2B):c.612G>A (p.Thr204=) rs369244943 0.00003
NM_004588.5(SCN2B):c.70+11_70+12insCT rs72544143

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