List of variants in gene FKRP reported as likely benign by Counsyl

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024301.5(FKRP):c.427C>A (p.Arg143Ser)	rs148206382	0.00359
NM_024301.5(FKRP):c.483C>T (p.Ala161=)	rs797045576	0.00002
NM_024301.5(FKRP):c.582G>A (p.Leu194=)	rs771223960	0.00001
NM_024301.5(FKRP):c.1056C>T (p.Arg352=)	rs886038682
NM_024301.5(FKRP):c.696G>T (p.Ala232=)	rs398124394
NM_024301.5(FKRP):c.708G>A (p.Leu236=)	rs886038683

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