List of variants in gene MYH7 reported as uncertain significance for Dilated Cardiomyopathy, Dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=)	rs200852418	0.00032
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=)	rs45523233	0.00016
NM_000257.4(MYH7):c.2028T>C (p.Asn676=)	rs145564868	0.00006
NM_000257.4(MYH7):c.3974C>T (p.Ala1325Val)	rs768393069	0.00004
NM_000257.4(MYH7):c.4158C>T (p.Leu1386=)	rs886050418	0.00004
NM_000257.4(MYH7):c.1983C>T (p.Asn661=)	rs146474860	0.00003
NM_000257.4(MYH7):c.540C>A (p.Ser180=)	rs369490861	0.00003
NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp)	rs779973529	0.00002
NM_000257.4(MYH7):c.733-3C>T	rs765068619	0.00002
NM_000257.4(MYH7):c.1749C>T (p.Ala583=)	rs758665829	0.00001
NM_000257.4(MYH7):c.2692C>T (p.Leu898=)	rs727504407	0.00001
NM_000257.4(MYH7):c.2922+6G>C	rs781192476	0.00001
NM_000257.4(MYH7):c.5606A>G (p.Asp1869Gly)	rs730880824	0.00001
NM_000257.4(MYH7):c.5726G>A (p.Arg1909Gln)	rs397516253	0.00001
NM_000257.4(MYH7):c.-39C>A	rs886050424
NM_000257.4(MYH7):c.-47G>T	rs886050425
NM_000257.4(MYH7):c.1671G>T (p.Leu557=)	rs149386750
NM_000257.4(MYH7):c.2968G>A (p.Ala990Thr)	rs753137666
NM_000257.4(MYH7):c.3148C>A (p.Arg1050=)	rs730880767
NM_000257.4(MYH7):c.4169+6T>G	rs886050417
NM_000257.4(MYH7):c.449C>G (p.Ala150Gly)	rs879196018
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=)	rs777053791
NM_000257.4(MYH7):c.5482G>A (p.Ala1828Thr)	rs886050415
NM_000257.4(MYH7):c.658A>C (p.Ile220Leu)	rs779190577
NM_000257.4(MYH7):c.895+12C>A	rs186276057

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