List of variants in gene ANO5 reported as uncertain significance for Miyoshi muscular dystrophy 3

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_213599.3(ANO5):c.424A>T (p.Thr142Ser)	rs757367942	0.00001
NM_213599.3(ANO5):c.1685T>C (p.Leu562Pro)	rs772361544
NM_213599.3(ANO5):c.1693_1715del (p.Phe565fs)	rs1554931773

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