List of variants in gene ZNF423 reported as uncertain significance by GeneDx

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)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001379286.1(ZNF423):c.1168T>C (p.Ser390Pro)	rs142835239	0.00063
NM_001379286.1(ZNF423):c.2683G>A (p.Gly895Ser)	rs147413663	0.00019
NM_001379286.1(ZNF423):c.1522C>T (p.Arg508Cys)	rs376465155	0.00009
NM_001379286.1(ZNF423):c.1217G>A (p.Arg406Gln)	rs375001883	0.00003
NM_001379286.1(ZNF423):c.2702C>T (p.Ala901Val)	rs1051021187	0.00003
NM_001379286.1(ZNF423):c.3301G>A (p.Ala1101Thr)	rs144425413	0.00003
NM_001379286.1(ZNF423):c.2480T>A (p.Ile827Asn)	rs529454153	0.00001
NM_001379286.1(ZNF423):c.2548G>A (p.Ala850Thr)	rs768539056	0.00001
NM_001379286.1(ZNF423):c.3467C>T (p.Pro1156Leu)	rs756742718	0.00001
NM_001379286.1(ZNF423):c.3106_3109del (p.Thr1036fs)
NM_001379286.1(ZNF423):c.3436C>G (p.His1146Asp)
NM_001379286.1(ZNF423):c.389G>T (p.Gly130Val)	rs1064794776
NM_001379286.1(ZNF423):c.395A>G (p.Asp132Gly)	rs2151888050
NM_001379286.1(ZNF423):c.495G>T (p.Glu165Asp)	rs1972856533

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