List of variants reported as benign for X-linked myopathy with excessive autophagy

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001017980.4(VMA21):c.225C>T (p.Ala75=)	rs139323488	0.00403
NM_001017980.4(VMA21):c.163+16T>G	rs188765636	0.00294
NM_001017980.4(VMA21):c.182A>G (p.Asn61Ser)	rs141926826	0.00208
NM_001017980.4(VMA21):c.165C>T (p.Gly55=)	rs146017753	0.00100
NM_001017980.4(VMA21):c.163+14C>T	rs373448097	0.00067
NM_001017980.4(VMA21):c.144T>G (p.Thr48=)	rs201487581	0.00017
NM_001017980.4(VMA21):c.255T>C (p.Tyr85=)	rs201565563	0.00010
NM_001017980.4(VMA21):c.76A>G (p.Thr26Ala)	rs143565725	0.00010
NM_001017980.4(VMA21):c.102A>G (p.Thr34=)	rs141809048	0.00003
NM_001017980.4(VMA21):c.252G>A (p.Val84=)	rs748982102	0.00001
NM_001017980.4(VMA21):c.164-11del	rs753508417
NM_001017980.4(VMA21):c.164-11dup	rs753508417
NM_001017980.4(VMA21):c.164-19G>T	rs773306168
NM_001363810.1(VMA21):c.19G>C (p.Gly7Arg)	rs176451

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