List of variants in gene combination LOC114827850, MYL2 studied for not specified

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.4-14C>T	rs12301951	0.03886
NM_000432.4(MYL2):c.4-14del	rs531661702	0.00105
NM_000432.4(MYL2):c.36C>T (p.Gly12=)	rs139794370	0.00072
NM_000432.4(MYL2):c.33G>A (p.Gly11=)	rs199742269	0.00011
NM_000432.4(MYL2):c.-46G>A	rs368048109	0.00010
NM_000432.4(MYL2):c.4-18G>A	rs730880933	0.00003
NM_000432.4(MYL2):c.-2C>T	rs730880938	0.00001
NM_000432.4(MYL2):c.31G>A (p.Gly11Arg)	rs397516402	0.00001
NM_000432.4(MYL2):c.63C>T (p.Phe21=)	rs779983470	0.00001
NM_000432.4(MYL2):c.13A>G (p.Lys5Glu)
NM_000432.4(MYL2):c.1A>G (p.Met1Val)	rs876661378
NM_000432.4(MYL2):c.45_46delinsT (p.Asn16fs)	rs727504300
NM_000432.4(MYL2):c.4G>A (p.Ala2Thr)	rs1060499882
NM_000432.4(MYL2):c.59T>A (p.Met20Lys)	rs113167834
NM_000432.4(MYL2):c.82G>A (p.Glu28Lys)	rs397516409
NM_000432.4(MYL2):c.84A>T (p.Glu28Asp)	rs397516410

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