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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 8

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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.1073C>T (p.Pro358Leu)	rs143031195	0.00011
NM_024301.5(FKRP):c.823C>T (p.Arg275Cys)	rs1247934219	0.00002
NM_024301.5(FKRP):c.1363G>T (p.Ala455Ser)	rs747785577	0.00001
NM_024301.5(FKRP):c.544T>C (p.Tyr182His)	rs753390261	0.00001
NM_024301.5(FKRP):c.854A>C (p.Glu285Ala)	rs963039919	0.00001
NM_024301.5(FKRP):c.968G>A (p.Arg323His)	rs1349031936	0.00001
NM_024301.5(FKRP):c.1016G>A (p.Arg339His)	rs1450841129

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