List of variants in gene MYOZ2 reported as likely benign for Hypertrophic cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_016599.5(MYOZ2):c.488T>C (p.Leu163Ser)	rs143345726	0.00058
NM_016599.5(MYOZ2):c.76+10A>G	rs372006344	0.00012
NM_016599.5(MYOZ2):c.303G>A (p.Ser101=)	rs527258961	0.00009
NM_016599.5(MYOZ2):c.245A>C (p.Asn82Thr)	rs149125238	0.00007
NM_016599.5(MYOZ2):c.313C>T (p.Pro105Ser)	rs748809573	0.00003
NM_016599.5(MYOZ2):c.376+9T>A	rs536009604	0.00003
NM_016599.5(MYOZ2):c.423C>T (p.Thr141=)	rs148220911	0.00003
NM_016599.5(MYOZ2):c.768C>A (p.Thr256=)	rs727503333	0.00003
NM_016599.5(MYOZ2):c.150C>T (p.Leu50=)	rs750398714	0.00002
NM_016599.5(MYOZ2):c.504T>C (p.Pro168=)	rs769668877	0.00002
NM_016599.5(MYOZ2):c.76+8T>C	rs773231367	0.00002
NM_016599.5(MYOZ2):c.123C>T (p.Asp41=)	rs753422262	0.00001
NM_016599.5(MYOZ2):c.207A>C (p.Thr69=)	rs774782954	0.00001
NM_016599.5(MYOZ2):c.309A>G (p.Gln103=)	rs1051191303	0.00001
NM_016599.5(MYOZ2):c.330C>T (p.Asn110=)	rs370237979	0.00001
NM_016599.5(MYOZ2):c.333C>T (p.Thr111=)	rs1553958625	0.00001
NM_016599.5(MYOZ2):c.391C>T (p.Leu131=)	rs1553959019	0.00001
NM_016599.5(MYOZ2):c.480G>A (p.Pro160=)	rs779726933	0.00001
NM_016599.5(MYOZ2):c.561-20T>C	rs771164968	0.00001
NM_016599.5(MYOZ2):c.561-6C>T	rs745918436	0.00001
NM_016599.5(MYOZ2):c.-15+11dup	rs58371596
NM_016599.5(MYOZ2):c.159T>C (p.Arg53=)	rs1578729988
NM_016599.5(MYOZ2):c.252T>C (p.Ser84=)
NM_016599.5(MYOZ2):c.303G>T (p.Ser101=)	rs527258961
NM_016599.5(MYOZ2):c.377-15T>C
NM_016599.5(MYOZ2):c.441C>T (p.Tyr147=)	rs1337507818
NM_016599.5(MYOZ2):c.447A>G (p.Gln149=)	rs200077093
NM_016599.5(MYOZ2):c.519T>C (p.Pro173=)
NM_016599.5(MYOZ2):c.546C>T (p.Tyr182=)
NM_016599.5(MYOZ2):c.552C>T (p.Ser184=)
NM_016599.5(MYOZ2):c.561-7C>T	rs863224424
NM_016599.5(MYOZ2):c.688C>T (p.Arg230Trp)	rs372215131
NM_016599.5(MYOZ2):c.705T>C (p.Thr235=)	rs1578374385
NM_016599.5(MYOZ2):c.77-18A>G
NM_016599.5(MYOZ2):c.77-9G>A	rs2149221401
NM_016599.5(MYOZ2):c.792A>G (p.Leu264=)	rs1355854115

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