List of variants in gene FXR1 reported as pathogenic for hereditary skeletal muscle 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_005087.4(FXR1):c.1603+725dup
NM_005087.4(FXR1):c.1603+733del	rs769011065
NM_005087.4(FXR1):c.1603+733dup
NM_005087.4(FXR1):c.1603+790_1603+793del	rs1577005361

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