ClinVar Miner

List of variants in gene NEDD4L reported as likely pathogenic for not provided

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_001144967.3(NEDD4L):c.2441G>A (p.Trp814Ter)	rs2146788855
NM_001144967.3(NEDD4L):c.623G>A (p.Arg208Gln)	rs2059194330

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