ClinVar Miner

List of variants in gene ZNF408 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_024741.3(ZNF408):c.1363C>T (p.His455Tyr)	rs373273223	0.00003
NM_024741.3(ZNF408):c.111del (p.Gln38fs)	rs2134505106

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