ClinVar Miner

List of variants reported as uncertain significance for schwannoma by Clinical Genomics Laboratory, Stanford 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.1904C>T (p.Pro635Leu)	rs148677674	0.00077
NM_006767.4(LZTR1):c.2062C>T (p.Arg688Cys)	rs587777178	0.00006
NM_006767.4(LZTR1):c.1806G>A (p.Val602=)	rs1157548960	0.00003

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