ClinVar Miner

List of variants in gene WDR62 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 53
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HGVS dbSNP
NM_001083961.2(WDR62):c.*5G>A rs61740165
NM_001083961.2(WDR62):c.1043+3A>G rs587784541
NM_001083961.2(WDR62):c.1095G>T (p.Leu365=) rs1555714428
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) rs139460397
NM_001083961.2(WDR62):c.1342T>A (p.Ser448Thr) rs144072948
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984
NM_001083961.2(WDR62):c.1486C>T (p.Arg496Trp) rs587784544
NM_001083961.2(WDR62):c.1509C>T (p.Asp503=) rs758922011
NM_001083961.2(WDR62):c.1534C>G (p.Arg512Gly) rs201993064
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) rs147875659
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1667G>T (p.Ser556Ile) rs780553760
NM_001083961.2(WDR62):c.1681A>T (p.Ile561Phe) rs587784545
NM_001083961.2(WDR62):c.1750A>C (p.Thr584Pro) rs76456648
NM_001083961.2(WDR62):c.1836+34G>T rs201569352
NM_001083961.2(WDR62):c.2057C>T (p.Thr686Ile) rs797046107
NM_001083961.2(WDR62):c.2490C>T (p.Asn830=) rs587784547
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) rs146274964
NM_001083961.2(WDR62):c.2566C>T (p.Arg856Cys) rs370558837
NM_001083961.2(WDR62):c.2584G>T (p.Gly862Cys) rs587784548
NM_001083961.2(WDR62):c.2666T>C (p.Met889Thr) rs139749569
NM_001083961.2(WDR62):c.2729T>A (p.Leu910Gln) rs911479602
NM_001083961.2(WDR62):c.2782C>T (p.Leu928=) rs12610991
NM_001083961.2(WDR62):c.2896G>A (p.Gly966Arg) rs587784550
NM_001083961.2(WDR62):c.2945G>A (p.Ser982Asn) rs11540047
NM_001083961.2(WDR62):c.2972A>T (p.Asp991Val) rs749528768
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=) rs757294519
NM_001083961.2(WDR62):c.3066G>A (p.Ser1022=) rs3746269
NM_001083961.2(WDR62):c.3247G>A (p.Val1083Met) rs375274868
NM_001083961.2(WDR62):c.32G>C (p.Arg11Pro) rs587784552
NM_001083961.2(WDR62):c.3336-5C>G rs587784555
NM_001083961.2(WDR62):c.3406C>G (p.Arg1136Gly) rs587784556
NM_001083961.2(WDR62):c.3515-7G>A rs368668756
NM_001083961.2(WDR62):c.3559G>A (p.Val1187Met) rs587784557
NM_001083961.2(WDR62):c.3573C>T (p.Asp1191=) rs1054040
NM_001083961.2(WDR62):c.3589C>A (p.Pro1197Thr) rs375708869
NM_001083961.2(WDR62):c.3611G>T (p.Gly1204Val) rs587784559
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168
NM_001083961.2(WDR62):c.3698C>G (p.Ser1233Cys) rs587784560
NM_001083961.2(WDR62):c.3786C>T (p.Gly1262=) rs148415080
NM_001083961.2(WDR62):c.3818C>T (p.Thr1273Ile) rs797046110
NM_001083961.2(WDR62):c.3948G>A (p.Gln1316=) rs4375791
NM_001083961.2(WDR62):c.4005C>A (p.Ser1335Arg) rs778940951
NM_001083961.2(WDR62):c.413G>A (p.Arg138His) rs199673795
NM_001083961.2(WDR62):c.4153G>A (p.Gly1385Ser) rs764128952
NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His) rs372272053
NM_001083961.2(WDR62):c.4312T>A (p.Leu1438Met) rs138814793
NM_001083961.2(WDR62):c.4381T>G (p.Trp1461Gly) rs61734910
NM_001083961.2(WDR62):c.4564G>A (p.Gly1522Arg) rs142600079
NM_001083961.2(WDR62):c.589G>A (p.Val197Ile) rs535488873
NM_001083961.2(WDR62):c.656G>A (p.Arg219His) rs375979418
NM_001083961.2(WDR62):c.82C>G (p.Arg28Gly) rs200283315
NM_001083961.2(WDR62):c.964G>C (p.Ala322Pro) rs587784561

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