ClinVar Miner

List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 1 by North West Genomic Laboratory Hub, Manchester University NHS Foundation Trust

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp)	rs145213771	0.00001
NM_000257.4(MYH7):c.727C>T (p.Arg243Cys)	rs397516265	0.00001
NM_000257.4(MYH7):c.1795G>T (p.Asp599Tyr)	rs2502296670

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