List of variants in gene MYLK2 reported as likely benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_033118.4(MYLK2):c.266G>A (p.Gly89Asp)	rs115398036	0.01365
NM_033118.4(MYLK2):c.173C>A (p.Ala58Asp)	rs138130914	0.00070
NM_033118.4(MYLK2):c.1590C>T (p.Asn530=)	rs374233822	0.00010
NM_033118.4(MYLK2):c.987G>A (p.Leu329=)	rs200155693	0.00009
NM_033118.4(MYLK2):c.261G>A (p.Ala87=)	rs374353729	0.00007
NM_033118.4(MYLK2):c.1086C>T (p.Ile362=)	rs188352991	0.00002
NM_033118.4(MYLK2):c.1137C>T (p.Thr379=)	rs759608229	0.00001
NM_033118.4(MYLK2):c.309A>T (p.Thr103=)	rs1269686595

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