ClinVar Miner

List of variants in gene VHL reported as uncertain significance for Von Hippel-Lindau syndrome; Nonpapillary renal cell carcinoma

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.5C>T (p.Pro2Leu)	rs111246617	0.00008
NM_000551.4(VHL):c.104C>T (p.Ala35Val)	rs587780536

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