ClinVar Miner

List of variants reported as uncertain significance for Hypertrophic cardiomyopathy 14 by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.2807C>T (p.Ala936Val)	rs199838024	0.00067
NM_002471.4(MYH6):c.5364G>A (p.Met1788Ile)	rs1890963680

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