ClinVar Miner

List of variants in gene NF2 reported as likely pathogenic for schwannoma

Included ClinVar conditions (11):

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_000268.4(NF2):c.1192_1193del (p.Leu398fs)
NM_000268.4(NF2):c.1340+1G>C
NM_000268.4(NF2):c.185T>C (p.Phe62Ser)	rs121434261

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