List of variants in gene MYL3 reported as likely benign by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NC_000003.12:g.46863682T>C	rs142106468	0.02371
NM_001406938.1(MYL3):c.-6-371G>A	rs2233263	0.01935
NM_000258.3(MYL3):c.307+86G>A	rs561570934	0.00155
NM_000258.3(MYL3):c.157+8G>C	rs777555567	0.00013
NM_000258.3(MYL3):c.*13+5G>C	rs200422816	0.00011
NM_000258.3(MYL3):c.516G>A (p.Leu172=)	rs367761724	0.00008
NM_000258.3(MYL3):c.420C>T (p.Phe140=)	rs201138698	0.00006
NM_000258.3(MYL3):c.246G>A (p.Ala82=)	rs368364468	0.00004
NM_000258.3(MYL3):c.130-10C>T	rs374988162	0.00003
NM_000258.3(MYL3):c.477G>A (p.Thr159=)	rs148365503	0.00003
NM_000258.3(MYL3):c.*27G>A	rs199474710	0.00001
NM_000258.3(MYL3):c.183C>T (p.Phe61=)	rs368118534	0.00001
NM_000258.3(MYL3):c.222G>A (p.Gly74=)	rs144543453	0.00001
NM_000258.3(MYL3):c.465C>T (p.His155=)	rs147125759	0.00001
NM_000258.3(MYL3):c.501C>T (p.Asp167=)	rs552824036	0.00001
NM_000258.3(MYL3):c.130-322C>A	rs77221239
NM_000258.3(MYL3):c.261C>T (p.Pro87=)	rs556711370
NM_000258.3(MYL3):c.36T>C (p.Asp12=)	rs138567316
NM_000258.3(MYL3):c.549C>T (p.Ile183=)	rs963631094

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