ClinVar Miner

List of variants in gene ZNF469 reported as likely benign for not provided

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Total variants: 45
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HGVS dbSNP
NM_001367624.1(ZNF469):c.10327G>C (p.Gly3443Arg) rs532857190
NM_001367624.1(ZNF469):c.10518G>A (p.Pro3506=) rs376379111
NM_001367624.1(ZNF469):c.10656G>A (p.Pro3552=) rs191234581
NM_001367624.1(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834
NM_001367624.1(ZNF469):c.10795G>T (p.Ala3599Ser) rs199760004
NM_001367624.1(ZNF469):c.11658G>C (p.Gln3886His) rs182269913
NM_001367624.1(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001367624.1(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001367624.1(ZNF469):c.1697C>T (p.Ala566Val) rs181785233
NM_001367624.1(ZNF469):c.1994C>T (p.Pro665Leu) rs184583062
NM_001367624.1(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145
NM_001367624.1(ZNF469):c.2666C>T (p.Ala889Val) rs145186655
NM_001367624.1(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481
NM_001367624.1(ZNF469):c.2814G>A (p.Ala938=) rs140480823
NM_001367624.1(ZNF469):c.2841G>A (p.Arg947=) rs150435442
NM_001367624.1(ZNF469):c.3341G>T (p.Arg1114Leu) rs568046708
NM_001367624.1(ZNF469):c.3773C>A (p.Ala1258Glu) rs141255631
NM_001367624.1(ZNF469):c.3950A>G (p.Lys1317Arg) rs772817384
NM_001367624.1(ZNF469):c.4363C>G (p.Leu1455Val) rs116532825
NM_001367624.1(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076
NM_001367624.1(ZNF469):c.4778C>T (p.Ser1593Leu) rs768864900
NM_001367624.1(ZNF469):c.4855G>A (p.Glu1619Lys) rs759327672
NM_001367624.1(ZNF469):c.4909C>T (p.Arg1637Trp) rs575820215
NM_001367624.1(ZNF469):c.498C>G (p.Leu166=) rs1555518472
NM_001367624.1(ZNF469):c.5087C>T (p.Pro1696Leu) rs115487796
NM_001367624.1(ZNF469):c.5145G>A (p.Arg1715=) rs577775261
NM_001367624.1(ZNF469):c.5548C>A (p.Pro1850Thr) rs199932922
NM_001367624.1(ZNF469):c.6333C>T (p.Ala2111=) rs1039243677
NM_001367624.1(ZNF469):c.6489G>A (p.Gln2163=) rs572299080
NM_001367624.1(ZNF469):c.6599C>T (p.Thr2200Ile) rs1465493306
NM_001367624.1(ZNF469):c.7267C>A (p.Pro2423Thr) rs199727372
NM_001367624.1(ZNF469):c.7675A>G (p.Lys2559Glu) rs146789160
NM_001367624.1(ZNF469):c.8409C>T (p.Pro2803=) rs376502074
NM_001367624.1(ZNF469):c.9018C>T (p.Ala3006=) rs1048591670
NM_001367624.1(ZNF469):c.9673G>A (p.Ala3225Thr) rs1046436333
NM_001367624.1(ZNF469):c.9696G>A (p.Thr3232=) rs573582117
NM_001367624.2(ZNF469):c.11449A>C (p.Arg3817=)
NM_001367624.2(ZNF469):c.11715C>T (p.Pro3905=)
NM_001367624.2(ZNF469):c.2908_2910GGC[2] (p.Gly972_Gly973del) rs775423936
NM_001367624.2(ZNF469):c.4946C>T (p.Ala1649Val)
NM_001367624.2(ZNF469):c.7425G>A (p.Glu2475=) rs1597212123
NM_001367624.2(ZNF469):c.8111A>C (p.Glu2704Ala) rs930146121
NM_001367624.2(ZNF469):c.891C>G (p.Phe297Leu) rs770483852
NM_001367624.2(ZNF469):c.9040G>A (p.Gly3014Arg) rs201438224
NM_001367624.2(ZNF469):c.9095_9109del (p.Leu3032_Thr3036del) rs281865162

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