List of variants reported as benign for myopathy, congenital, with structured cores and z-line abnormalities

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.242-84G>A	rs1341865	0.99335
NM_001103.4(ACTN2):c.351T>C (p.Ile117=)	rs1341864	0.99334
NM_001103.4(ACTN2):c.448+73G>A	rs1341862	0.93228
NM_001103.4(ACTN2):c.378C>T (p.Asn126=)	rs1341863	0.93032
NM_001103.4(ACTN2):c.2526+33A>G	rs2282366	0.85706
NM_001103.4(ACTN2):c.877-8C>G	rs2288601	0.77958
NM_001103.4(ACTN2):c.1107+33A>C	rs2288602	0.50667
NM_001103.4(ACTN2):c.241+131C>T	rs2275399	0.45532
NM_001103.4(ACTN2):c.697+33G>A	rs819640	0.39452
NM_001103.4(ACTN2):c.1053G>C (p.Lys351Asn)
NM_001103.4(ACTN2):c.877-42C>T	rs7527525

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