List of variants in gene DYSF reported as benign for Miyoshi myopathy

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.1881T>C (p.Asp627=)	rs2303596	0.71202
NM_001130987.2(DYSF):c.2637A>T (p.Ser879=)	rs2288355	0.69367
NM_001130987.2(DYSF):c.1449+13C>T	rs4852801	0.60553
NM_001130987.2(DYSF):c.4062C>A (p.Ile1354=)	rs2303606	0.47852
NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=)	rs11558179	0.18595

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