List of variants reported as likely benign for Ventricular fibrillation

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000152.5(GAA):c.676C>G (p.Leu226Val)	rs113085339	0.00193
NM_001267550.2(TTN):c.95653G>A (p.Ala31885Thr)	rs72648263	0.00070
NM_005751.5(AKAP9):c.3580G>A (p.Ala1194Thr)	rs139965373	0.00035
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)	rs141122361	0.00034
NM_001267550.2(TTN):c.89708C>G (p.Thr29903Ser)	rs72648240	0.00013
NM_000218.3(KCNQ1):c.160_168dup (p.Ile54_Pro56dup)	rs397515877
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys)	rs141764279

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