ClinVar Miner

List of variants in gene NSDHL reported as benign 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.132T>G (p.Gly44=)	rs5969919	0.83345
NM_015922.3(NSDHL):c.1054C>T (p.Leu352=)	rs142351862	0.00444

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