ClinVar Miner

List of variants in gene WDR11 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018117.12(WDR11):c.1153del (p.Leu385fs)
NM_018117.12(WDR11):c.1280T>G (p.Leu427Ter)
NM_018117.12(WDR11):c.3033_3036del	rs760973100

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