List of variants in gene MYH7 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.3972+62_3972+63insC	rs34598192	0.42217
NM_000257.4(MYH7):c.77C>T (p.Ala26Val)	rs186964570	0.00021
NM_000257.4(MYH7):c.5786C>T (p.Thr1929Met)	rs730880918	0.00010
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro)	rs372731424	0.00010
NM_000257.4(MYH7):c.2183C>T (p.Ala728Val)	rs121913644	0.00009
NM_000257.4(MYH7):c.115G>A (p.Val39Met)	rs376160714	0.00006
NM_000257.4(MYH7):c.5326A>G (p.Ser1776Gly)	rs369437262	0.00006
NM_000257.4(MYH7):c.5779A>T (p.Ile1927Phe)	rs767300277	0.00006
NM_000257.4(MYH7):c.3301G>A (p.Gly1101Ser)	rs367546859	0.00002
NM_000257.4(MYH7):c.4052C>T (p.Thr1351Met)	rs370403289	0.00002
NM_000257.4(MYH7):c.5561C>T (p.Thr1854Met)	rs372381770	0.00002
NM_000257.4(MYH7):c.632C>T (p.Pro211Leu)	rs727503277	0.00002
NM_000257.4(MYH7):c.733-3C>T	rs765068619	0.00002
NM_000257.4(MYH7):c.958G>A (p.Val320Met)	rs376897125	0.00002
NM_000257.4(MYH7):c.2681A>G (p.Glu894Gly)	rs397516161	0.00001
NM_000257.4(MYH7):c.3235C>T (p.Arg1079Trp)	rs192722540	0.00001
NM_000257.4(MYH7):c.3407G>A (p.Arg1136His)	rs730880905	0.00001
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp)	rs145213771	0.00001
NM_000257.4(MYH7):c.5500G>A (p.Ala1834Thr)	rs143362532	0.00001
NM_000257.4(MYH7):c.5536C>T (p.Arg1846Cys)	rs12590294	0.00001
NM_000257.4(MYH7):c.1547A>G (p.Asp516Gly)	rs1595086171
NM_000257.4(MYH7):c.1820G>A (p.Gly607Asp)	rs869025479
NM_000257.4(MYH7):c.2795T>C (p.Met932Thr)	rs202097576
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys)	rs141764279
NM_000257.4(MYH7):c.536A>C (p.Glu179Ala)	rs869025476
NM_000257.4(MYH7):c.793A>T (p.Thr265Ser)	rs730880157

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