List of variants in gene ZNF408 reported as likely benign for retinal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_024741.3(ZNF408):c.1557C>T (p.Thr519=)	rs148867575	0.00019
NM_024741.3(ZNF408):c.892G>A (p.Gly298Ser)	rs371633363	0.00004
NM_024741.3(ZNF408):c.377G>A (p.Ser126Asn)	rs536561101	0.00003
NM_024741.3(ZNF408):c.1992G>A (p.Glu664=)	rs762663282	0.00001
NM_024741.3(ZNF408):c.704C>G (p.Pro235Arg)

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