List of variants in gene ZNF469 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.1489G>A (p.Gly497Arg)	rs28723506	0.09509
NM_001367624.2(ZNF469):c.6470G>A (p.Arg2157Lys)	rs13334190	0.09442
NM_001367624.2(ZNF469):c.1697C>T (p.Ala566Val)	rs181785233	0.00939
NM_001367624.2(ZNF469):c.7079C>T (p.Pro2360Leu)	rs76389306	0.00188
NM_001367624.2(ZNF469):c.10700G>A (p.Gly3567Glu)	rs199610834	0.00185
NM_001367624.2(ZNF469):c.5644G>A (p.Ala1882Thr)	rs74032866	0.00185
NM_001367624.2(ZNF469):c.946G>A (p.Glu316Lys)	rs368772806	0.00085
NM_001367624.2(ZNF469):c.2035G>A (p.Glu679Lys)	rs551591362	0.00080
NM_001367624.2(ZNF469):c.99G>A (p.Pro33=)	rs273585631	0.00002
NM_001367624.2(ZNF469):c.10325G>C (p.Arg3442Thr)	rs199528724
NM_001367624.2(ZNF469):c.10794G>A (p.Gly3598=)
NM_001367624.2(ZNF469):c.3003C>T (p.Ala1001=)	rs993032767

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