ClinVar Miner

List of variants reported as likely pathogenic for bone benign neoplasm by Genetic Services Laboratory, University of Chicago

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.1114del (p.Val372fs)	rs587784222
NM_015922.3(NSDHL):c.595C>T (p.Arg199Cys)	rs587784223
NM_015922.3(NSDHL):c.727G>A (p.Val243Met)	rs587784224

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