List of variants in gene DYSF reported as pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.2697+1G>A	rs140108514	0.00046
NM_001130987.2(DYSF):c.4307G>A (p.Gly1436Asp)	rs398123787	0.00004
NM_001130987.2(DYSF):c.2929C>T (p.Arg977Trp)	rs202218890	0.00002
NM_001130987.2(DYSF):c.4873C>T (p.Arg1625Ter)	rs398123789	0.00001
NM_001130987.2(DYSF):c.3498_3499delinsAA (p.Tyr1166_Gly1167delinsTer)	rs398123781
NM_001130987.2(DYSF):c.4551G>A (p.Trp1517Ter)	rs766016391

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