List of variants reported as likely pathogenic for long QT syndrome by Centogene AG - the Rare Disease Company

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.6043G>A (p.Val2015Met)	rs762981322	0.00004
NM_000719.7(CACNA1C):c.2451del (p.Ala818fs)	rs2153231721

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