ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 59
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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.10361G>A (p.Arg3454Gln) rs75288466 0.00769
NM_001367624.2(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481 0.00528
NM_001367624.2(ZNF469):c.9125G>A (p.Arg3042His) rs150598363 0.00461
NM_001127464.2(ZNF469):c.-18C>A rs568661500 0.00399
NM_001367624.2(ZNF469):c.6489G>A (p.Gln2163=) rs572299080 0.00320
NM_001367624.2(ZNF469):c.6036G>A (p.Thr2012=) rs149961653 0.00229
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.10710G>A (p.Ala3570=) rs548910839 0.00106
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.1689C>T (p.Phe563=) rs751136702 0.00031
NM_001367624.2(ZNF469):c.1932G>A (p.Thr644=) rs539996728 0.00007
NM_001367624.2(ZNF469):c.1911A>G (p.Pro637=) rs373169260 0.00006
NM_001367624.2(ZNF469):c.4463C>T (p.Pro1488Leu) rs565994438 0.00006
NM_001367624.2(ZNF469):c.8409C>T (p.Pro2803=) rs376502074 0.00006
NM_001367624.2(ZNF469):c.9087C>T (p.Asp3029=) rs780843955 0.00006
NM_001367624.2(ZNF469):c.6984G>A (p.Ser2328=) rs764025593 0.00005
NM_001367624.2(ZNF469):c.4611C>T (p.Gly1537=) rs775651401 0.00004
NM_001367624.2(ZNF469):c.11022G>A (p.Ala3674=) rs1002770054 0.00003
NM_001367624.2(ZNF469):c.8577C>T (p.Phe2859=) rs1057524534 0.00003
NM_001367624.2(ZNF469):c.9849C>T (p.Asp3283=) rs949391158 0.00003
NM_001367624.2(ZNF469):c.11691G>A (p.Gln3897=) rs1322051909 0.00002
NM_001367624.2(ZNF469):c.2415C>T (p.Ala805=) rs961899310 0.00002
NM_001367624.2(ZNF469):c.4155C>T (p.Leu1385=) rs747930231 0.00002
NM_001367624.2(ZNF469):c.4755G>A (p.Pro1585=) rs370447132 0.00002
NM_001367624.2(ZNF469):c.6204G>A (p.Leu2068=) rs575840696 0.00002
NM_001367624.2(ZNF469):c.99G>A (p.Pro33=) rs273585631 0.00002
NM_001367624.2(ZNF469):c.10713G>A (p.Leu3571=) rs981130895 0.00001
NM_001367624.2(ZNF469):c.10860C>T (p.Phe3620=) rs1230771468 0.00001
NM_001367624.2(ZNF469):c.11070C>T (p.Ser3690=) rs1272116933 0.00001
NM_001367624.2(ZNF469):c.135C>T (p.Thr45=) rs538850431 0.00001
NM_001367624.2(ZNF469):c.1809C>T (p.Ser603=) rs748014455 0.00001
NM_001367624.2(ZNF469):c.2508T>C (p.Asp836=) rs1447365697 0.00001
NM_001367624.2(ZNF469):c.4440G>A (p.Leu1480=) rs755586686 0.00001
NM_001367624.2(ZNF469):c.6090C>T (p.Thr2030=) rs754253956 0.00001
NM_001367624.2(ZNF469):c.7089C>T (p.Pro2363=) rs779456576 0.00001
NM_001367624.2(ZNF469):c.7140A>G (p.Pro2380=) rs1396219207 0.00001
NM_001367624.2(ZNF469):c.8214A>C (p.Ala2738=) rs1459194051 0.00001
NM_001367624.2(ZNF469):c.1005G>A (p.Leu335=) rs1555518581
NM_001367624.2(ZNF469):c.10325G>C (p.Arg3442Thr) rs199528724
NM_001367624.2(ZNF469):c.10325G>T (p.Arg3442Met) rs199528724
NM_001367624.2(ZNF469):c.10328G>C (p.Gly3443Ala) rs140056980
NM_001367624.2(ZNF469):c.10377G>C (p.Pro3459=) rs910515287
NM_001367624.2(ZNF469):c.10794G>A (p.Gly3598=)
NM_001367624.2(ZNF469):c.1095G>T (p.Pro365=) rs534477237
NM_001367624.2(ZNF469):c.11184C>G (p.Pro3728=) rs1041924878
NM_001367624.2(ZNF469):c.222G>A (p.Lys74=) rs998864240
NM_001367624.2(ZNF469):c.2733C>T (p.Pro911=) rs1278230482
NM_001367624.2(ZNF469):c.3003C>T (p.Ala1001=) rs993032767
NM_001367624.2(ZNF469):c.3072C>T (p.Ser1024=) rs1219175594
NM_001367624.2(ZNF469):c.3468G>A (p.Glu1156=) rs1555519130
NM_001367624.2(ZNF469):c.3654G>C (p.Ser1218=) rs1555519186
NM_001367624.2(ZNF469):c.7956T>C (p.Ser2652=) rs898700599
NM_001367624.2(ZNF469):c.8072A>G (p.Gln2691Arg) rs573064293

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