ClinVar Miner

List of variants reported as uncertain significance for schwannoma by Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.2471T>C (p.Leu824Pro)	rs752239353	0.00001
NM_003073.5(SMARCB1):c.158G>T (p.Arg53Leu)	rs779769475
NM_006767.4(LZTR1):c.1559C>T (p.Pro520Leu)	rs1569157089

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