ClinVar Miner

List of variants in gene WDR35 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP
NM_001006657.2(WDR35):c.*1006G>A rs80292673
NM_001006657.2(WDR35):c.*1038C>G rs145549829
NM_001006657.2(WDR35):c.*1062G>A rs778834686
NM_001006657.2(WDR35):c.*1253C>G rs368665906
NM_001006657.2(WDR35):c.*1270C>T rs568999408
NM_001006657.2(WDR35):c.*1461A>C rs886055400
NM_001006657.2(WDR35):c.*1582C>T rs757203175
NM_001006657.2(WDR35):c.*1668A>C rs191316348
NM_001006657.2(WDR35):c.*1681A>G rs188310451
NM_001006657.2(WDR35):c.*1934A>G rs886055399
NM_001006657.2(WDR35):c.*2029_*2032GTCT[1] rs566446459
NM_001006657.2(WDR35):c.*2288C>T rs886055398
NM_001006657.2(WDR35):c.*2341G>C rs886055397
NM_001006657.2(WDR35):c.*2559A>G rs751743368
NM_001006657.2(WDR35):c.*2619C>T rs565144558
NM_001006657.2(WDR35):c.*2622A>G rs558837510
NM_001006657.2(WDR35):c.*2623T>C rs538967974
NM_001006657.2(WDR35):c.*2725G>T rs886055396
NM_001006657.2(WDR35):c.*2726A>G rs886055395
NM_001006657.2(WDR35):c.*2748G>T rs886055394
NM_001006657.2(WDR35):c.*2797G>A rs528776835
NM_001006657.2(WDR35):c.*2887T>C rs749198501
NM_001006657.2(WDR35):c.*2962C>T rs886055393
NM_001006657.2(WDR35):c.*2989C>T rs886055392
NM_001006657.2(WDR35):c.*2990G>T rs781556463
NM_001006657.2(WDR35):c.*3225G>A rs189820516
NM_001006657.2(WDR35):c.*3235C>A rs186978842
NM_001006657.2(WDR35):c.*3269G>A rs886055391
NM_001006657.2(WDR35):c.*380G>A rs886055401
NM_001006657.2(WDR35):c.*531T>A rs187092318
NM_001006657.2(WDR35):c.*563T>G rs561642193
NM_001006657.2(WDR35):c.*573A>T rs140069324
NM_001006657.2(WDR35):c.*601A>G rs182037850
NM_001006657.2(WDR35):c.*763T>C rs560228088
NM_001006657.2(WDR35):c.*795C>T rs190700326
NM_001006657.2(WDR35):c.*813A>T rs148210550
NM_001006657.2(WDR35):c.*998A>G rs530093062
NM_001006657.2(WDR35):c.1029T>C (p.Thr343=) rs536150588
NM_001006657.2(WDR35):c.1053T>C (p.Pro351=) rs74385826
NM_001006657.2(WDR35):c.1058G>C (p.Arg353Pro) rs76623454
NM_001006657.2(WDR35):c.1089G>A (p.Thr363=) rs79829477
NM_001006657.2(WDR35):c.10T>C (p.Tyr4His)
NM_001006657.2(WDR35):c.1183A>T (p.Asn395Tyr) rs143343508
NM_001006657.2(WDR35):c.1215A>G (p.Thr405=) rs144673252
NM_001006657.2(WDR35):c.1226C>T (p.Thr409Met) rs143430766
NM_001006657.2(WDR35):c.1283A>T (p.Asp428Val) rs371757004
NM_001006657.2(WDR35):c.1624C>G (p.Leu542Val) rs148242353
NM_001006657.2(WDR35):c.1669C>T (p.Arg557Cys) rs549077153
NM_001006657.2(WDR35):c.1730C>T (p.Thr577Met) rs780159239
NM_001006657.2(WDR35):c.1786G>A (p.Val596Ile) rs748998292
NM_001006657.2(WDR35):c.1904T>G (p.Ile635Ser) rs139252416
NM_001006657.2(WDR35):c.206G>A (p.Gly69Asp) rs765513105
NM_001006657.2(WDR35):c.2098C>T (p.Arg700Cys) rs140196566
NM_001006657.2(WDR35):c.2140A>G (p.Thr714Ala) rs886055405
NM_001006657.2(WDR35):c.215-4C>G rs369080910
NM_001006657.2(WDR35):c.2162G>T (p.Arg721Leu)
NM_001006657.2(WDR35):c.2170G>A (p.Asp724Asn) rs778732776
NM_001006657.2(WDR35):c.2253C>T (p.Phe751=) rs535522970
NM_001006657.2(WDR35):c.2295C>T (p.Asp765=) rs147206032
NM_001006657.2(WDR35):c.2301-11T>G rs745664606
NM_001006657.2(WDR35):c.24+4A>G rs780961583
NM_001006657.2(WDR35):c.2433T>C (p.Ala811=) rs886055404
NM_001006657.2(WDR35):c.2525A>G (p.Tyr842Cys) rs886055403
NM_001006657.2(WDR35):c.2548A>G (p.Ile850Val) rs763618858
NM_001006657.2(WDR35):c.2613G>A (p.Met871Ile) rs201443916
NM_001006657.2(WDR35):c.2705T>C (p.Val902Ala)
NM_001006657.2(WDR35):c.2711T>C (p.Leu904Ser) rs151047156
NM_001006657.2(WDR35):c.2810A>G (p.Tyr937Cys) rs75602337
NM_001006657.2(WDR35):c.2869G>A (p.Glu957Lys) rs779009587
NM_001006657.2(WDR35):c.2989A>G (p.Ser997Gly) rs886055402
NM_001006657.2(WDR35):c.2998-4G>T rs199696980
NM_001006657.2(WDR35):c.3017G>T (p.Gly1006Val) rs376284452
NM_001006657.2(WDR35):c.3059C>G (p.Thr1020Arg) rs201153804
NM_001006657.2(WDR35):c.308G>C (p.Gly103Ala) rs886055406
NM_001006657.2(WDR35):c.3091C>T (p.His1031Tyr) rs1553316264
NM_001006657.2(WDR35):c.3154+3G>A rs200042577
NM_001006657.2(WDR35):c.3203A>G (p.Tyr1068Cys) rs541910371
NM_001006657.2(WDR35):c.3226T>A (p.Cys1076Ser) rs200258619
NM_001006657.2(WDR35):c.3312G>C (p.Gln1104His) rs148436608
NM_001006657.2(WDR35):c.3431G>A (p.Gly1144Glu) rs1558317742
NM_001006657.2(WDR35):c.3445G>A (p.Glu1149Lys) rs978909925
NM_001006657.2(WDR35):c.355C>T (p.Arg119Cys) rs140308808
NM_001006657.2(WDR35):c.664C>G (p.Pro222Ala) rs1553322982
NM_001006657.2(WDR35):c.765C>T (p.Tyr255=) rs117255034
NM_001006657.2(WDR35):c.766G>A (p.Val256Ile) rs745580829
NM_001006657.2(WDR35):c.770T>C (p.Val257Ala) rs142955097
NM_001006657.2(WDR35):c.798C>T (p.Ser266=) rs141118263
NM_001006657.2(WDR35):c.847G>A (p.Val283Met) rs576085633
NM_001006657.2(WDR35):c.853A>T (p.Ile285Phe)

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