List of variants in gene combination LOC130067016, LZTR1 reported as likely pathogenic for schwannoma

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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.115G>T (p.Glu39Ter)	rs762434811	0.00001
NM_006767.4(LZTR1):c.18_30del (p.Ser6fs)
NM_006767.4(LZTR1):c.46del (p.Leu16fs)	rs35574094

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