List of variants in gene ZNF469 reported as uncertain significance by Eurofins NTD LLC (GA)

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.2717C>T (p.Pro906Leu)	rs77951481	0.00528
NM_001367624.2(ZNF469):c.11277C>T (p.Ser3759=)	rs372634401	0.00490
NM_001367624.2(ZNF469):c.2841G>A (p.Arg947=)	rs150435442	0.00334
NM_001367624.2(ZNF469):c.1615A>T (p.Ser539Cys)	rs189476639	0.00283
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.10700G>A (p.Gly3567Glu)	rs199610834	0.00185
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.8788G>T (p.Asp2930Tyr)	rs76792613	0.00133
NM_001367624.2(ZNF469):c.9516C>T (p.Ala3172=)	rs577913880	0.00131
NM_001367624.2(ZNF469):c.2297G>A (p.Arg766Gln)	rs144492145	0.00111
NM_001367624.2(ZNF469):c.1483C>T (p.Pro495Ser)	rs202205643	0.00073
NM_001367624.2(ZNF469):c.1088C>T (p.Ser363Leu)	rs771000169	0.00058
NM_001367624.2(ZNF469):c.4952A>G (p.Gln1651Arg)	rs773925755	0.00034
NM_001367624.2(ZNF469):c.7981G>A (p.Gly2661Ser)	rs138259179	0.00026
NM_001367624.2(ZNF469):c.248C>T (p.Pro83Leu)	rs775103017	0.00019
NM_001367624.2(ZNF469):c.8489G>C (p.Gly2830Ala)	rs541325052	0.00016
NM_001367624.2(ZNF469):c.4422G>A (p.Ala1474=)	rs368877287	0.00014
NM_001367624.2(ZNF469):c.11771C>T (p.Thr3924Met)	rs139259830	0.00011
NM_001367624.2(ZNF469):c.4829G>A (p.Arg1610His)	rs567038987	0.00007
NM_001367624.2(ZNF469):c.10582G>A (p.Glu3528Lys)	rs758708056	0.00003
NM_001367624.2(ZNF469):c.11278G>A (p.Glu3760Lys)	rs547014159	0.00003
NM_001367624.2(ZNF469):c.4427G>A (p.Arg1476Lys)	rs763632522	0.00002
NM_001367624.2(ZNF469):c.2017G>A (p.Ala673Thr)	rs770623245	0.00001
NM_001367624.2(ZNF469):c.4556C>T (p.Ser1519Leu)	rs767278971	0.00001
NM_001367624.2(ZNF469):c.8425C>G (p.Pro2809Ala)	rs794727257	0.00001
NM_001367624.2(ZNF469):c.8477A>G (p.Asp2826Gly)	rs886043475	0.00001
NM_001367624.2(ZNF469):c.9131C>T (p.Thr3044Met)	rs273585626	0.00001
NM_001367624.2(ZNF469):c.10683C>T (p.Ala3561=)	rs794727258
NM_001367624.2(ZNF469):c.457C>G (p.Pro153Ala)	rs532620482
NM_001367624.2(ZNF469):c.5340C>G (p.Pro1780=)	rs184374078
NM_001367624.2(ZNF469):c.725_726delinsTT (p.Ser242Ile)	rs886043704
NM_001367624.2(ZNF469):c.9663C>T (p.Ser3221=)	rs1555520265

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