ClinVar Miner

List of variants in gene WDR62 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001083961.2(WDR62):c.2381C>G (p.Pro794Arg) rs149431376 0.00084
NM_001083961.2(WDR62):c.303C>A (p.Asn101Lys) rs139371621 0.00073
NM_001083961.2(WDR62):c.4564G>A (p.Gly1522Arg) rs142600079 0.00053
NM_001083961.2(WDR62):c.3058G>A (p.Ala1020Thr) rs144120866 0.00040
NM_001083961.2(WDR62):c.82C>T (p.Arg28Trp) rs200283315 0.00038
NM_001083961.2(WDR62):c.203T>C (p.Ile68Thr) rs148615988 0.00031
NM_001083961.2(WDR62):c.2873A>T (p.Tyr958Phe) rs376554781 0.00031
NM_001083961.2(WDR62):c.3589C>A (p.Pro1197Thr) rs375708869 0.00030
NM_001083961.2(WDR62):c.3248T>C (p.Val1083Ala) rs143600070 0.00026
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) rs147875659 0.00022
NM_001083961.2(WDR62):c.3035C>T (p.Pro1012Leu) rs1006271908 0.00014
NM_001083961.2(WDR62):c.824C>T (p.Ser275Leu) rs202014178 0.00014
NM_001083961.2(WDR62):c.4186C>T (p.Arg1396Cys) rs778841660 0.00013
NM_001083961.2(WDR62):c.16T>G (p.Ser6Ala) rs573013010 0.00011
NM_001083961.2(WDR62):c.1696G>A (p.Val566Met) rs145392484 0.00010
NM_001083961.2(WDR62):c.4546G>A (p.Val1516Met) rs369708392 0.00009
NM_001083961.2(WDR62):c.2765G>A (p.Arg922His) rs749718711 0.00007
NM_001083961.2(WDR62):c.1480G>A (p.Gly494Arg) rs587784543 0.00006
NM_001083961.2(WDR62):c.3937G>A (p.Val1313Met) rs144440621 0.00006
NM_001083961.2(WDR62):c.3558C>T (p.Ser1186=) rs111889921 0.00005
NM_001083961.2(WDR62):c.3232G>A (p.Ala1078Thr) rs373781801 0.00004
NM_001083961.2(WDR62):c.3733C>A (p.Leu1245Met) rs763947043 0.00004
NM_001083961.2(WDR62):c.4307G>A (p.Arg1436His) rs146018199 0.00004
NM_001083961.2(WDR62):c.785G>A (p.Arg262Gln) rs563462202 0.00004
NM_001083961.2(WDR62):c.3412G>A (p.Gly1138Arg) rs750117864 0.00003
NM_001083961.2(WDR62):c.1479C>T (p.Ala493=) rs150656878 0.00002
NM_001083961.2(WDR62):c.1521G>A (p.Leu507=) rs778207666 0.00002
NM_001083961.2(WDR62):c.1765G>A (p.Ala589Thr) rs149192461 0.00002
NM_001083961.2(WDR62):c.2887G>A (p.Val963Met) rs113046428 0.00002
NM_001083961.2(WDR62):c.3576G>C (p.Arg1192Ser) rs201995586 0.00002
NM_001083961.2(WDR62):c.413G>A (p.Arg138His) rs199673795 0.00002
NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His) rs372272053 0.00002
NM_001083961.2(WDR62):c.1129G>A (p.Val377Met) rs761204875 0.00001
NM_001083961.2(WDR62):c.1151A>C (p.Tyr384Ser) rs758675905 0.00001
NM_001083961.2(WDR62):c.1238A>T (p.Tyr413Phe) rs1265156638 0.00001
NM_001083961.2(WDR62):c.1471G>A (p.Val491Met) rs768534840 0.00001
NM_001083961.2(WDR62):c.1530C>T (p.Gly510=) rs751638362 0.00001
NM_001083961.2(WDR62):c.1627T>G (p.Ser543Ala) rs141895633 0.00001
NM_001083961.2(WDR62):c.2111C>T (p.Ser704Leu) rs750547223 0.00001
NM_001083961.2(WDR62):c.3306G>T (p.Gln1102His) rs1353495263 0.00001
NM_001083961.2(WDR62):c.3463-9T>C rs1346976662 0.00001
NM_001083961.2(WDR62):c.3527C>T (p.Thr1176Met) rs774735502 0.00001
NM_001083961.2(WDR62):c.3809C>T (p.Thr1270Ile) rs760672019 0.00001
NM_001083961.2(WDR62):c.3851C>A (p.Ala1284Asp) rs1161069528 0.00001
NM_001083961.2(WDR62):c.4153G>A (p.Gly1385Ser) rs764128952 0.00001
NM_001083961.2(WDR62):c.4499A>G (p.Asp1500Gly) rs771866189 0.00001
NM_001083961.2(WDR62):c.4543G>A (p.Ala1515Thr) rs750893805 0.00001
NM_001083961.2(WDR62):c.4561C>T (p.Arg1521Trp) rs748425985 0.00001
NM_001083961.2(WDR62):c.4572A>C (p.Ter1524Cys) rs1973671414 0.00001
NM_001083961.2(WDR62):c.655C>T (p.Arg219Cys) rs924844578 0.00001
NM_001083961.2(WDR62):c.979T>C (p.Tyr327His) rs781278130 0.00001
NM_001083961.2(WDR62):c.1005C>G (p.His335Gln) rs2145626544
NM_001083961.2(WDR62):c.1334G>T (p.Ser445Ile)
NM_001083961.2(WDR62):c.1393G>A (p.Val465Met)
NM_001083961.2(WDR62):c.1535G>T (p.Arg512Leu) rs375417358
NM_001083961.2(WDR62):c.1667G>A (p.Ser556Asn) rs780553760
NM_001083961.2(WDR62):c.2345A>C (p.Tyr782Ser)
NM_001083961.2(WDR62):c.2711C>T (p.Pro904Leu)
NM_001083961.2(WDR62):c.2989G>A (p.Ala997Thr) rs1973348017
NM_001083961.2(WDR62):c.3092G>A (p.Gly1031Asp)
NM_001083961.2(WDR62):c.3247G>C (p.Val1083Leu) rs375274868
NM_001083961.2(WDR62):c.3276C>G (p.Phe1092Leu) rs551013571
NM_001083961.2(WDR62):c.4006G>A (p.Ala1336Thr) rs150966716
NM_001083961.2(WDR62):c.4272del (p.Gln1425fs)
NM_001083961.2(WDR62):c.4397T>A (p.Leu1466Gln) rs2145889410
NM_001083961.2(WDR62):c.4550G>A (p.Arg1517Gln)
NM_001083961.2(WDR62):c.562-3C>G
NM_001083961.2(WDR62):c.685_687del (p.Ser229del) rs2145586990
NM_001083961.2(WDR62):c.952C>T (p.Arg318Cys) rs1046543015

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.