List of variants in gene FXR1 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005087.4(FXR1):c.247A>G (p.Lys83Glu)	rs1721862059
NM_005087.4(FXR1):c.28G>T (p.Gly10Cys)
NM_005087.4(FXR1):c.346A>G (p.Asn116Asp)	rs1721905984

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