List of variants reported as benign for Hypertrophic cardiomyopathy 10

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Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.132T>C (p.Ile44=)	rs2301610	0.08171
NM_000432.4(MYL2):c.4-14C>T	rs12301951	0.04173
NM_000432.4(MYL2):c.381G>A (p.Ala127=)	rs2233261	0.00558
NM_000432.4(MYL2):c.170-19T>C	rs115522476	0.00399
NM_000432.4(MYL2):c.279G>A (p.Ala93=)	rs28645088	0.00131
NM_000432.4(MYL2):c.4-14del	rs531661702	0.00105
NM_000432.4(MYL2):c.36C>T (p.Gly12=)	rs139794370	0.00076
NM_000432.4(MYL2):c.353+12C>A	rs186323458	0.00022
NM_000432.4(MYL2):c.243G>T (p.Val81=)	rs368851472	0.00015
NM_000432.4(MYL2):c.33G>A (p.Gly11=)	rs199742269	0.00011
NM_000432.4(MYL2):c.3+9A>G	rs201763406	0.00007
NM_000432.4(MYL2):c.275-7G>A	rs373241541	0.00006
NM_000432.4(MYL2):c.456C>T (p.Tyr152=)	rs199815885	0.00005
NM_000432.4(MYL2):c.353+16G>A	rs572363699	0.00004
NM_000432.4(MYL2):c.274+16_274+17insTC	rs200007468
NM_000432.4(MYL2):c.353+20del	rs3833910
NM_000432.4(MYL2):c.4-13dup	rs756245911
NM_000432.4(MYL2):c.4-3del	rs886048961
NM_000432.4(MYL2):c.4-8del
NM_000432.4(MYL2):c.402+9del

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