List of variants in gene NSDHL reported as not provided for CK syndrome

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_015922.3(NSDHL):c.1098dup (p.Arg367fs)	rs121909834
NM_015922.3(NSDHL):c.455G>A (p.Gly152Asp)	rs2521798824
NM_015922.3(NSDHL):c.693GAA[1] (p.Lys232del)	rs121909833

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