List of variants in gene DYSF reported as uncertain significance by Pars Genome Lab

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.2956A>T (p.Met986Leu)	rs144636654	0.00112
NM_001130987.2(DYSF):c.2982C>T (p.Asn994=)	rs142404822	0.00098
NM_001130987.2(DYSF):c.5143G>T (p.Ala1715Ser)	rs141137410	0.00046
NM_001130987.2(DYSF):c.6116G>A (p.Arg2039Gln)	rs115407852	0.00019
NM_001130987.2(DYSF):c.1287C>T (p.Ala429=)	rs769254776	0.00004

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