List of variants in gene combination DYSF, LOC122787137 reported as uncertain significance for muscle tissue disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.3946A>G (p.Ile1316Val)	rs121908954	0.00491
NM_001130987.2(DYSF):c.3943A>G (p.Arg1315Gly)	rs535831045	0.00004
NM_001130987.2(DYSF):c.3928-10T>C	rs1558589946
NM_001130987.2(DYSF):c.3957G>A (p.Glu1319=)	rs781449138

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