List of variants in gene MYH7 reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1727A>G (p.His576Arg)	rs727504238	0.00002
NM_000257.4(MYH7):c.958G>A (p.Val320Met)	rs376897125	0.00002
NM_000257.4(MYH7):c.1370T>C (p.Ile457Thr)	rs397516103	0.00001
NM_000257.4(MYH7):c.1491G>T (p.Glu497Asp)	rs267606911	0.00001
NM_000257.4(MYH7):c.4130C>T (p.Thr1377Met)	rs397516201	0.00001
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp)	rs145213771	0.00001
NM_000257.4(MYH7):c.428G>A (p.Arg143Gln)	rs397516209	0.00001
NM_000257.4(MYH7):c.709C>T (p.Arg237Trp)	rs45516091	0.00001
NM_000257.4(MYH7):c.727C>T (p.Arg243Cys)	rs397516265	0.00001
NM_000257.4(MYH7):c.3134G>T (p.Arg1045Leu)	rs397516178
NM_000257.4(MYH7):c.428G>C (p.Arg143Pro)	rs397516209
NM_000257.4(MYH7):c.715G>A (p.Asp239Asn)	rs397516264

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