List of variants reported as uncertain significance for CK syndrome

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.44G>A (p.Arg15Gln)	rs200748828	0.00002
NM_015922.3(NSDHL):c.1010A>G (p.Tyr337Cys)
NM_015922.3(NSDHL):c.1054C>G (p.Leu352Val)	rs142351862
NM_015922.3(NSDHL):c.457G>A (p.Val153Ile)

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