ClinVar Miner

Variants in gene ZNF469 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 61
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001367624.2(ZNF469):c.1471G>A (p.Ala491Thr) rs117555121 0.00632
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.751C>A (p.Pro251Thr) rs540655479 0.00166
NM_001367624.2(ZNF469):c.10330G>C (p.Gly3444Arg) rs569602115 0.00135
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.2699C>T (p.Pro900Leu) rs273585618 0.00093
NM_001367624.2(ZNF469):c.9676C>A (p.His3226Asn) rs867530230 0.00081
NM_001367624.2(ZNF469):c.5006C>T (p.Ala1669Val) rs200070902 0.00070
NM_001367624.2(ZNF469):c.11697A>C (p.Arg3899Ser) rs561879014 0.00063
NM_001367624.2(ZNF469):c.7573C>G (p.Pro2525Ala) rs574478833 0.00061
NM_001367624.2(ZNF469):c.8860T>C (p.Trp2954Arg) rs557063759 0.00061
NM_001367624.2(ZNF469):c.1088C>T (p.Ser363Leu) rs771000169 0.00058
NM_001367624.2(ZNF469):c.697G>A (p.Asp233Asn) rs538330967 0.00053
NM_001367624.2(ZNF469):c.8344C>T (p.His2782Tyr) rs553227769 0.00051
NM_001367624.2(ZNF469):c.8401G>C (p.Gly2801Arg) rs555522972 0.00043
NM_001367624.2(ZNF469):c.10762G>A (p.Gly3588Arg) rs750481489 0.00041
NM_001367624.2(ZNF469):c.4456G>A (p.Asp1486Asn) rs373777402 0.00036
NM_001367624.2(ZNF469):c.8996G>T (p.Gly2999Val) rs273585625 0.00034
NM_001367624.2(ZNF469):c.10717G>A (p.Gly3573Arg) rs183149417 0.00026
NM_001367624.2(ZNF469):c.6179C>A (p.Ser2060Tyr) rs273585623 0.00026
NM_001367624.2(ZNF469):c.7981G>A (p.Gly2661Ser) rs138259179 0.00026
NM_001367624.2(ZNF469):c.5915G>T (p.Gly1972Val) rs573931575 0.00021
NM_001367624.2(ZNF469):c.248C>T (p.Pro83Leu) rs775103017 0.00018
NM_001367624.2(ZNF469):c.5144G>A (p.Arg1715Lys) rs281865149 0.00017
NM_001367624.2(ZNF469):c.11033G>A (p.Ser3678Asn) rs781084356 0.00013
NM_001367624.2(ZNF469):c.4316C>T (p.Thr1439Met) rs752630858 0.00012
NM_001367624.2(ZNF469):c.14G>A (p.Arg5His) rs762382027 0.00011
NM_001367624.2(ZNF469):c.266A>G (p.Lys89Arg) rs1022368248 0.00009
NM_001367624.2(ZNF469):c.3452C>T (p.Ala1151Val) rs755348435 0.00009
NM_001367624.2(ZNF469):c.7195C>T (p.Pro2399Ser) rs759032227 0.00008
NM_001367624.2(ZNF469):c.1663G>A (p.Asp555Asn) rs749179728 0.00006
NM_001367624.2(ZNF469):c.4463C>T (p.Pro1488Leu) rs565994438 0.00006
NM_001367624.2(ZNF469):c.6236C>T (p.Ser2079Phe) rs765190704 0.00006
NM_001367624.2(ZNF469):c.8458G>A (p.Gly2820Ser) rs761603858 0.00006
NM_001367624.2(ZNF469):c.8806G>A (p.Glu2936Lys) rs762301873 0.00006
NM_001367624.2(ZNF469):c.356G>A (p.Arg119His) rs759962057 0.00005
NM_001367624.2(ZNF469):c.4276G>A (p.Glu1426Lys) rs868174994 0.00004
NM_001367624.2(ZNF469):c.1768G>A (p.Glu590Lys) rs571115191 0.00001
NM_001367624.2(ZNF469):c.10199C>T (p.Pro3400Leu) rs281165933
NM_001367624.2(ZNF469):c.10328G>T (p.Gly3443Val) rs140056980
NM_001367624.2(ZNF469):c.10331G>T (p.Gly3444Val) rs530393871
NM_001367624.2(ZNF469):c.10437G>A (p.Met3479Ile)
NM_001367624.2(ZNF469):c.11767C>T (p.Arg3923Trp)
NM_001367624.2(ZNF469):c.1363C>A (p.Pro455Thr)
NM_001367624.2(ZNF469):c.4088C>G (p.Pro1363Arg) rs953923193
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.5539G>A (p.Ala1847Thr)
NM_001367624.2(ZNF469):c.6739G>T (p.Asp2247Tyr)
NM_001367624.2(ZNF469):c.6751A>G (p.Arg2251Gly)
NM_001367624.2(ZNF469):c.9368G>A (p.Arg3123His) rs536601676
NM_001367624.2(ZNF469):c.9703G>A (p.Ala3235Thr)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.