Variants in gene FKRP with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_024301.5(FKRP):c.898G>A (p.Val300Met)	rs563033008	0.00031
NM_024301.5(FKRP):c.731G>A (p.Arg244His)	rs764641619	0.00010
NM_024301.5(FKRP):c.926A>G (p.Tyr309Cys)	rs104894679	0.00001
NM_024301.5(FKRP):c.400C>T (p.Arg134Trp)	rs104894690
NM_024301.5(FKRP):c.586G>C (p.Gly196Arg)	rs759875552

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