ClinVar Miner

List of variants reported as uncertain significance for Long QT syndrome 1 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.575G>A (p.Arg192His)	rs199472698	0.00001
NM_000218.3(KCNQ1):c.1694A>C (p.Gln565Pro)	rs1846716972
NM_000218.3(KCNQ1):c.173C>A (p.Ala58Asp)

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