List of variants in gene MYL3 reported as likely pathogenic for 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000258.3(MYL3):c.466G>A (p.Val156Met)	rs199474707	0.00004
NM_000258.3(MYL3):c.235G>A (p.Val79Ile)	rs150634297	0.00001
NM_000258.3(MYL3):c.281G>A (p.Arg94His)	rs199474703	0.00001
NM_000258.3(MYL3):c.427G>A (p.Glu143Lys)	rs104893750	0.00001
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp)	rs139794067
NM_000258.3(MYL3):c.170C>G (p.Ala57Gly)	rs139794067
NM_000258.3(MYL3):c.383G>A (p.Gly128Asp)	rs869025485
NM_000258.3(MYL3):c.446T>C (p.Met149Thr)	rs202141423
NM_000258.3(MYL3):c.447G>A (p.Met149Ile)	rs730880162
NM_000258.3(MYL3):c.447G>T (p.Met149Ile)	rs730880162
NM_000258.3(MYL3):c.463C>G (p.His155Asp)	rs199474706
NM_000258.3(MYL3):c.466G>T (p.Val156Leu)	rs199474707

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