List of variants reported as benign for Hypertrophic cardiomyopathy by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.706A>G (p.Ser236Gly)	rs3729989	0.09621
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	rs3729823	0.00861
NM_000256.3(MYBPC3):c.2498C>T (p.Ala833Val)	rs3729952	0.00756
NM_000256.3(MYBPC3):c.977G>A (p.Arg326Gln)	rs34580776	0.00376
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp)	rs193068692	0.00047
NM_000432.4(MYL2):c.37G>A (p.Ala13Thr)	rs104894363	0.00020

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