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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_024301.5(FKRP):c.341C>G (p.Ala114Gly)	rs143793528	0.00910
NM_024301.5(FKRP):c.235G>A (p.Val79Met)	rs104894683	0.00435
NM_024301.5(FKRP):c.1177G>A (p.Val393Ile)	rs140679502	0.00150
NM_024301.5(FKRP):c.567C>T (p.Pro189=)	rs201454433	0.00144
NM_024301.5(FKRP):c.606G>A (p.Leu202=)	rs140084192	0.00066
NM_024301.5(FKRP):c.885C>T (p.Arg295=)	rs769005880	0.00022
NM_024301.5(FKRP):c.54T>A (p.Leu18=)	rs565563742	0.00008

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