List of variants in gene MYLK2 reported as uncertain significance 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_033118.4(MYLK2):c.524C>A (p.Thr175Asn)	rs202084078	0.00066
NM_033118.4(MYLK2):c.834T>A (p.Asn278Lys)	rs41293104	0.00044
NM_033118.4(MYLK2):c.463A>T (p.Ile155Phe)	rs140233643	0.00006
NM_033118.4(MYLK2):c.-3C>T	rs1452504056	0.00003
NM_033118.4(MYLK2):c.1626C>A (p.Asn542Lys)	rs368444888	0.00003
NM_033118.4(MYLK2):c.1694T>C (p.Met565Thr)	rs727503306	0.00003
NM_033118.4(MYLK2):c.364G>C (p.Asp122His)	rs748134754	0.00002
NM_033118.4(MYLK2):c.1183C>T (p.Leu395Phe)	rs1568631895
NM_033118.4(MYLK2):c.1564G>A (p.Val522Ile)	rs747657397
NM_033118.4(MYLK2):c.1613C>T (p.Pro538Leu)	rs1600414450
NM_033118.4(MYLK2):c.167C>T (p.Ala56Val)	rs751084569
NM_033118.4(MYLK2):c.1711-4C>T	rs372190501
NM_033118.4(MYLK2):c.402G>T (p.Glu134Asp)	rs768092962

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