List of variants in gene VHL reported as likely benign for epithelial neoplasm

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.267C>A (p.Leu89=)	rs755794553	0.00002
NM_000551.4(VHL):c.-10C>T	rs1192379474

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