List of variants in gene MYL2 reported as benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.132T>C (p.Ile44=)	rs2301610	0.08171
NM_000432.4(MYL2):c.381G>A (p.Ala127=)	rs2233261	0.00558
NM_000432.4(MYL2):c.170-19T>C	rs115522476	0.00399
NM_000432.4(MYL2):c.279G>A (p.Ala93=)	rs28645088	0.00131
NM_000432.4(MYL2):c.353+16G>A	rs572363699	0.00004
NM_000432.4(MYL2):c.274+16_274+17insTC	rs200007468
NM_000432.4(MYL2):c.274+9GT[10]	rs142567411
NM_000432.4(MYL2):c.353+20del	rs3833910
NM_000432.4(MYL2):c.353+51C>A	rs2233260

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