List of variants in gene combination LOC114827850, MYL2 reported as uncertain significance for Cardiovascular phenotype

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.37G>A (p.Ala13Thr)	rs104894363	0.00020
NM_000432.4(MYL2):c.49G>A (p.Val17Met)	rs730880943	0.00003
NM_000432.4(MYL2):c.-2C>T	rs730880938	0.00001
NM_000432.4(MYL2):c.20A>G (p.Lys7Arg)	rs1344327792	0.00001
NM_000432.4(MYL2):c.23A>G (p.Lys8Arg)	rs886039195	0.00001
NM_000432.4(MYL2):c.28G>A (p.Ala10Thr)	rs730880942	0.00001
NM_000432.4(MYL2):c.34G>T (p.Gly12Cys)	rs730880937	0.00001
NM_000432.4(MYL2):c.93+5G>A	rs2071703564	0.00001
NM_000432.4(MYL2):c.-1C>T	rs2499816647
NM_000432.4(MYL2):c.3+1G>T	rs730880948
NM_000432.4(MYL2):c.4-5C>T	rs374870836
NM_000432.4(MYL2):c.40A>C (p.Asn14His)	rs2499814987
NM_000432.4(MYL2):c.41A>G (p.Asn14Ser)	rs2071704259
NM_000432.4(MYL2):c.42C>A (p.Asn14Lys)	rs878853980
NM_000432.4(MYL2):c.42C>G (p.Asn14Lys)
NM_000432.4(MYL2):c.47A>G (p.Asn16Ser)	rs2071704153
NM_000432.4(MYL2):c.47del (p.Asn16fs)	rs781431079
NM_000432.4(MYL2):c.4G>A (p.Ala2Thr)	rs1060499882
NM_000432.4(MYL2):c.50T>C (p.Val17Ala)	rs2136777356
NM_000432.4(MYL2):c.53T>C (p.Phe18Ser)	rs730880944
NM_000432.4(MYL2):c.61T>G (p.Phe21Val)	rs2499814919
NM_000432.4(MYL2):c.64G>T (p.Glu22Ter)	rs104894368
NM_000432.4(MYL2):c.73C>G (p.Gln25Glu)	rs2499814879
NM_000432.4(MYL2):c.7C>T (p.Pro3Ser)	rs763957786
NM_000432.4(MYL2):c.83_93+1del	rs1490618460
NM_000432.4(MYL2):c.92_93+1del	rs751392310

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