ClinVar Miner

Variants in gene WDR62 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 50
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HGVS dbSNP gnomAD frequency
NM_001083961.2(WDR62):c.*5G>A rs61740165 0.00745
NM_001083961.2(WDR62):c.4312-5T>G rs182467995 0.00215
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) rs146274964 0.00161
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) rs148667984 0.00138
NM_001083961.2(WDR62):c.2666T>C (p.Met889Thr) rs139749569 0.00137
NM_001083961.2(WDR62):c.3440A>G (p.Tyr1147Cys) rs146867414 0.00113
NM_001083961.2(WDR62):c.2211-4G>A rs202109439 0.00096
NM_001083961.2(WDR62):c.2381C>G (p.Pro794Arg) rs149431376 0.00084
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) rs117887683 0.00078
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) rs139460397 0.00077
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) rs146180208 0.00075
NM_001083961.2(WDR62):c.303C>A (p.Asn101Lys) rs139371621 0.00073
NM_001083961.2(WDR62):c.1769-7C>T rs137919897 0.00071
NM_001083961.2(WDR62):c.922A>G (p.Ile308Val) rs146229976 0.00070
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) rs139946168 0.00066
NM_001083961.2(WDR62):c.4564G>A (p.Gly1522Arg) rs142600079 0.00053
NM_001083961.2(WDR62):c.477G>A (p.Ala159=) rs146485488 0.00051
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186 0.00041
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.2976G>A (p.Ser992=) rs757294519 0.00035
NM_001083961.2(WDR62):c.203T>C (p.Ile68Thr) rs148615988 0.00031
NM_001083961.2(WDR62):c.2211-8C>T rs369077520 0.00031
NM_001083961.2(WDR62):c.820T>G (p.Tyr274Asp) rs746156911 0.00021
NM_001083961.2(WDR62):c.1233+7C>G rs537771936 0.00017
NM_001083961.2(WDR62):c.189G>T (p.Glu63Asp) rs201053854 0.00016
NM_001083961.2(WDR62):c.3087C>T (p.Cys1029=) rs141344823 0.00015
NM_001083961.2(WDR62):c.824C>T (p.Ser275Leu) rs202014178 0.00014
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=) rs373906889 0.00013
NM_001083961.2(WDR62):c.391-10C>T rs201568145 0.00013
NM_001083961.2(WDR62):c.4122C>T (p.Gly1374=) rs773948810 0.00008
NM_001083961.2(WDR62):c.1509C>T (p.Asp503=) rs758922011 0.00005
NM_001083961.2(WDR62):c.3558C>T (p.Ser1186=) rs111889921 0.00005
NM_001083961.2(WDR62):c.1977C>T (p.Asn659=) rs79238222 0.00004
NM_001083961.2(WDR62):c.3733C>A (p.Leu1245Met) rs763947043 0.00004
NM_001083961.2(WDR62):c.4144C>T (p.Pro1382Ser) rs772768990 0.00004
NM_001083961.2(WDR62):c.4329G>A (p.Gln1443=) rs771131709 0.00004
NM_001083961.2(WDR62):c.1479C>T (p.Ala493=) rs150656878 0.00002
NM_001083961.2(WDR62):c.1642+9G>A rs112789274 0.00001
NM_001083961.2(WDR62):c.2040T>C (p.His680=) rs765451882 0.00001
NM_001083961.2(WDR62):c.3463-9T>C rs1346976662 0.00001
NM_001083961.2(WDR62):c.525C>T (p.Tyr175=) rs779093591 0.00001
NM_001083961.2(WDR62):c.1233+15del rs373693641
NM_001083961.2(WDR62):c.1233+15dup rs373693641
NM_001083961.2(WDR62):c.156C>G (p.Ser52=) rs398123559
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1959-10A>C rs767989054
NM_001083961.2(WDR62):c.3162G>A (p.Pro1054=) rs200232641
NM_001083961.2(WDR62):c.3271_3273del (p.His1091del) rs794727435
NM_001083961.2(WDR62):c.3641C>T (p.Thr1214Ile) rs752898108

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