ClinVar Miner

List of variants reported as not provided for schwannoma by GenomeConnect - Invitae Patient Insights Network

Included ClinVar conditions (11):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.1912C>T (p.Arg638Cys)	rs1213535694	0.00001
NM_006767.4(LZTR1):c.2284C>T (p.Gln762Ter)	rs1924868328

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