List of variants in gene MYL2 reported as likely benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.279G>A (p.Ala93=)	rs28645088	0.00131
NM_000432.4(MYL2):c.342G>A (p.Leu114=)	rs199572927	0.00032
NM_000432.4(MYL2):c.243G>T (p.Val81=)	rs368851472	0.00015
NM_000432.4(MYL2):c.359G>A (p.Arg120Gln)	rs192057022	0.00009
NM_000432.4(MYL2):c.387G>A (p.Arg129=)	rs774686046	0.00006
NM_000432.4(MYL2):c.456C>T (p.Tyr152=)	rs199815885	0.00005
NM_000432.4(MYL2):c.375G>A (p.Thr125=)	rs190020833	0.00003
NM_000432.4(MYL2):c.216G>A (p.Glu72=)	rs376506450	0.00002
NM_000432.4(MYL2):c.222G>A (p.Pro74=)	rs372644111	0.00002
NM_000432.4(MYL2):c.355G>A (p.Val119Ile)	rs730880940	0.00002
NM_000432.4(MYL2):c.468G>A (p.Val156=)	rs137984206	0.00002
NM_000432.4(MYL2):c.474C>T (p.Ile158=)	rs1423130699	0.00002
NM_000432.4(MYL2):c.138G>A (p.Lys46=)	rs1267967428	0.00001
NM_000432.4(MYL2):c.156C>A (p.Thr52=)	rs761358011	0.00001
NM_000432.4(MYL2):c.303C>T (p.Asn101=)	rs1317472220	0.00001
NM_000432.4(MYL2):c.354C>T (p.Tyr118=)	rs750193844	0.00001
NM_000432.4(MYL2):c.408C>T (p.Asp136=)	rs1356499130	0.00001
NM_000432.4(MYL2):c.483C>T (p.His161=)	rs886039108	0.00001
NM_000432.4(MYL2):c.141C>T (p.Asn47=)	rs199474808
NM_000432.4(MYL2):c.144T>C (p.Asp48=)
NM_000432.4(MYL2):c.180C>T (p.Asn60=)
NM_000432.4(MYL2):c.375G>C (p.Thr125=)	rs190020833
NM_000432.4(MYL2):c.420C>T (p.Ala140=)	rs369489428
NM_000432.4(MYL2):c.426C>T (p.Phe142=)	rs1592798603
NM_000432.4(MYL2):c.429C>G (p.Pro143=)	rs374328118
NM_000432.4(MYL2):c.435C>T (p.Asp145=)	rs766907447
NM_000432.4(MYL2):c.438G>T (p.Val146=)
NM_000432.4(MYL2):c.444C>T (p.Gly148=)	rs1555257596
NM_000432.4(MYL2):c.463C>T (p.Leu155=)	rs1592798503
NM_000432.4(MYL2):c.486A>C (p.Gly162=)	rs1177510197

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