List of variants in gene ZNF469 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.7675A>G (p.Lys2559Glu)	rs146789160	0.00403
NM_001367624.2(ZNF469):c.2841G>A (p.Arg947=)	rs150435442	0.00334
NM_001367624.2(ZNF469):c.6489G>A (p.Gln2163=)	rs572299080	0.00320
NM_001367624.2(ZNF469):c.1615A>T (p.Ser539Cys)	rs189476639	0.00283
NM_001367624.2(ZNF469):c.4198C>A (p.Pro1400Thr)	rs145158875	0.00255
NM_001367624.2(ZNF469):c.4472C>T (p.Thr1491Met)	rs375045076	0.00255
NM_001367624.2(ZNF469):c.7267C>A (p.Pro2423Thr)	rs199727372	0.00222
NM_001367624.2(ZNF469):c.10888C>T (p.Arg3630Cys)	rs200668806	0.00179
NM_001367624.2(ZNF469):c.1609G>A (p.Val537Met)	rs184458982	0.00172
NM_001367624.2(ZNF469):c.2270T>G (p.Leu757Arg)	rs753664726	0.00140
NM_001367624.2(ZNF469):c.725G>T (p.Ser242Ile)	rs536586591	0.00135
NM_001367624.2(ZNF469):c.726C>T (p.Ser242=)	rs555256402	0.00135
NM_001367624.2(ZNF469):c.2297G>A (p.Arg766Gln)	rs144492145	0.00111
NM_001367624.2(ZNF469):c.10656G>A (p.Pro3552=)	rs191234581	0.00106
NM_001367624.2(ZNF469):c.1896G>A (p.Ser632=)	rs554795578	0.00090
NM_001367624.2(ZNF469):c.1483C>T (p.Pro495Ser)	rs202205643	0.00073
NM_001367624.2(ZNF469):c.5006C>T (p.Ala1669Val)	rs200070902	0.00070
NM_001367624.2(ZNF469):c.9555C>G (p.Ala3185=)	rs273585636	0.00052
NM_001367624.2(ZNF469):c.8344C>T (p.His2782Tyr)	rs553227769	0.00051
NM_001367624.2(ZNF469):c.3321G>A (p.Arg1107=)	rs763826959	0.00045
NM_001367624.2(ZNF469):c.7850G>A (p.Arg2617Gln)	rs200019229	0.00017
NM_001367624.2(ZNF469):c.723T>C (p.Asn241=)	rs150745096	0.00005
NM_001367624.2(ZNF469):c.2322C>T (p.Pro774=)	rs1477401083	0.00002
NM_001367624.2(ZNF469):c.10328G>C (p.Gly3443Ala)	rs140056980
NM_001367624.2(ZNF469):c.5340C>G (p.Pro1780=)	rs184374078
NM_001367624.2(ZNF469):c.5340C>T (p.Pro1780=)	rs184374078

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