ClinVar Miner

List of variants in gene WDR81 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001163809.2(WDR81):c.1189C>T (p.Arg397Ter)	rs1200455844	0.00001
NM_001163809.2(WDR81):c.3771T>G (p.Tyr1257Ter)	rs1484029774

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