List of variants in gene MYL3 reported as 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000258.3(MYL3):c.307+37A>C	rs2227294	0.34149
NM_000258.3(MYL3):c.129+44G>T	rs936175	0.30333
NM_000258.3(MYL3):c.*89G>A	rs1042973	0.17840
NM_000258.3(MYL3):c.308-257G>A	rs1463395	0.12307
NM_000258.3(MYL3):c.482-100C>T	rs3729704	0.08920
NM_000258.3(MYL3):c.129+193C>A	rs28763895	0.02328
NM_000258.3(MYL3):c.69C>T (p.Pro23=)	rs2233264	0.02058
NM_000258.3(MYL3):c.130-14G>T	rs192329378	0.00198
NM_000258.3(MYL3):c.81T>C (p.Pro27=)	rs147584015	0.00133
NM_000258.3(MYL3):c.-27C>T	rs201910884	0.00079
NM_000258.3(MYL3):c.559+6C>T	rs199474709	0.00077
NM_000258.3(MYL3):c.482-14C>A	rs201780962	0.00048
NM_000258.3(MYL3):c.307+15C>T	rs184025552	0.00036
NM_000258.3(MYL3):c.482-17C>T	rs201289145	0.00030
NM_000258.3(MYL3):c.307+16G>A	rs759754750	0.00029
NM_000258.3(MYL3):c.559+19G>A	rs552393482	0.00012
NM_000258.3(MYL3):c.*9C>T	rs202234617	0.00006
NM_000258.2(MYL3):c.-90C>T	rs372094875	0.00004
NM_000258.3(MYL3):c.219C>T (p.Tyr73=)	rs780500137	0.00002
NM_000258.3(MYL3):c.381A>C (p.Thr127=)	rs758267230	0.00001
NM_000258.3(MYL3):c.*13+40G>T	rs2106904116
NM_000258.3(MYL3):c.249G>T (p.Leu83=)	rs2106909829
NM_000258.3(MYL3):c.307+56T>G	rs200593962
NM_000258.3(MYL3):c.411G>T (p.Leu137=)	rs2233265
NM_000258.3(MYL3):c.477G>T (p.Thr159=)	rs148365503
NM_000258.3(MYL3):c.560-30T>C	rs760655445

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