List of variants in gene combination LOC114827850, MYL2 reported as benign

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.4-77A>T	rs10849917	0.13009
NM_000432.4(MYL2):c.4-14C>T	rs12301951	0.03886
NM_000432.4(MYL2):c.3+97C>T	rs2233258	0.02346
NM_000432.4(MYL2):c.3+33C>T	rs138179416	0.00988
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.37G>A (p.Ala13Thr)	rs104894363	0.00020
NM_000432.4(MYL2):c.-27G>A	rs374106618	0.00013
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.3+9A>G	rs201763406	0.00007
NM_000432.4(MYL2):c.4-18G>A	rs730880933	0.00003
NM_000432.4(MYL2):c.-45G>A	rs2136779435
NM_000432.4(MYL2):c.3+218del	rs3216816
NM_000432.4(MYL2):c.4-13dup	rs756245911
NM_000432.4(MYL2):c.4-3del	rs886048961
NM_000432.4(MYL2):c.4-8del	rs756245911

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