List of variants in gene combination LOC114827850, MYL2 reported by Color Diagnostics, LLC DBA Color Health

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.4-14C>T	rs12301951	0.04173
NM_000432.4(MYL2):c.4-14del	rs531661702	0.00105
NM_000432.4(MYL2):c.36C>T (p.Gly12=)	rs139794370	0.00076
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.48C>T (p.Asn16=)	rs552004172	0.00003
NM_000432.4(MYL2):c.49G>A (p.Val17Met)	rs730880943	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.-2C>T	rs730880938	0.00001
NM_000432.4(MYL2):c.28G>A (p.Ala10Thr)	rs730880942	0.00001
NM_000432.4(MYL2):c.31G>A (p.Gly11Arg)	rs397516402	0.00001
NM_000432.4(MYL2):c.34G>T (p.Gly12Cys)	rs730880937	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.-12G>A	rs886048962
NM_000432.4(MYL2):c.-16_-13del	rs2071716291
NM_000432.4(MYL2):c.-3A>G	rs1313785501
NM_000432.4(MYL2):c.11A>G (p.Lys4Arg)
NM_000432.4(MYL2):c.31G>C (p.Gly11Arg)	rs397516402
NM_000432.4(MYL2):c.34G>A (p.Gly12Ser)	rs730880937
NM_000432.4(MYL2):c.35G>T (p.Gly12Val)	rs762584624
NM_000432.4(MYL2):c.4-13dup	rs756245911
NM_000432.4(MYL2):c.4-3C>G
NM_000432.4(MYL2):c.4-9T>A	rs758688050
NM_000432.4(MYL2):c.49del (p.Val17fs)	rs2136777366
NM_000432.4(MYL2):c.56C>G (p.Ser19Cys)	rs2071704028
NM_000432.4(MYL2):c.58A>G (p.Met20Val)	rs199474816
NM_000432.4(MYL2):c.64G>A (p.Glu22Lys)	rs104894368
NM_000432.4(MYL2):c.78C>T (p.Ile26=)	rs755926255
NM_000432.4(MYL2):c.92_93+1del	rs751392310
NM_000432.4(MYL2):c.93+5G>A	rs2071703564

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