List of variants in gene combination LOC114827850, MYL2 reported as likely benign for cardiovascular disorder

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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: 30

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.-28C>T	rs377590769	0.00041
NM_000432.4(MYL2):c.37G>A (p.Ala13Thr)	rs104894363	0.00020
NM_000432.4(MYL2):c.33G>A (p.Gly11=)	rs199742269	0.00011
NM_000432.4(MYL2):c.4-18G>A	rs730880933	0.00003
NM_000432.4(MYL2):c.48C>T (p.Asn16=)	rs552004172	0.00003
NM_000432.4(MYL2):c.30C>T (p.Ala10=)	rs752641375	0.00002
NM_000432.4(MYL2):c.4-8T>C	rs750730703	0.00002
NM_000432.4(MYL2):c.42C>T (p.Asn14=)	rs878853980	0.00002
NM_000432.4(MYL2):c.4-19C>T	rs1566150502	0.00001
NM_000432.4(MYL2):c.4-5C>G	rs374870836	0.00001
NM_000432.4(MYL2):c.4G>T (p.Ala2Ser)	rs1060499882	0.00001
NM_000432.4(MYL2):c.63C>T (p.Phe21=)	rs779983470	0.00001
NM_000432.4(MYL2):c.93+15T>C	rs754871718	0.00001
NM_000432.4(MYL2):c.-3A>G	rs1313785501
NM_000432.4(MYL2):c.18A>G (p.Ala6=)
NM_000432.4(MYL2):c.3+14C>T
NM_000432.4(MYL2):c.3+20G>A
NM_000432.4(MYL2):c.30C>A (p.Ala10=)	rs752641375
NM_000432.4(MYL2):c.30C>G (p.Ala10=)
NM_000432.4(MYL2):c.4-13dup	rs756245911
NM_000432.4(MYL2):c.4-5C>T	rs374870836
NM_000432.4(MYL2):c.4-6_4-5delinsTT	rs2136777520
NM_000432.4(MYL2):c.4-8T>A
NM_000432.4(MYL2):c.4-9T>A	rs758688050
NM_000432.4(MYL2):c.4-9T>C
NM_000432.4(MYL2):c.45_46delinsT (p.Asn16fs)	rs727504300
NM_000432.4(MYL2):c.72C>G (p.Thr24=)	rs2136777292
NM_000432.4(MYL2):c.78C>T (p.Ile26=)	rs755926255
NM_000432.4(MYL2):c.93+14T>G
NM_000432.4(MYL2):c.93+9A>G	rs201580029

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