ClinVar Miner

List of variants in gene WDR62 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) rs146180912
NM_001083961.2(WDR62):c.1233+11C>A
NM_001083961.2(WDR62):c.1233+13C>T rs76130844
NM_001083961.2(WDR62):c.1315T>G (p.Phe439Val) rs75230537
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) rs62109744
NM_001083961.2(WDR62):c.1470C>T (p.Asp490=) rs45567532
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=) rs2301734
NM_001083961.2(WDR62):c.1642+8C>T rs143309981
NM_001083961.2(WDR62):c.1643-10C>T rs4806263
NM_001083961.2(WDR62):c.180G>A (p.Val60=) rs61742664
NM_001083961.2(WDR62):c.186C>T (p.Leu62=) rs11538454
NM_001083961.2(WDR62):c.2271G>A (p.Leu757=) rs61494900
NM_001083961.2(WDR62):c.2281C>T (p.His761Tyr) rs61744321
NM_001083961.2(WDR62):c.2334-6C>A rs138928852
NM_001083961.2(WDR62):c.2521-13G>C rs79646208
NM_001083961.2(WDR62):c.2549T>C (p.Leu850Ser) rs2285745
NM_001083961.2(WDR62):c.2991C>T (p.Ala997=) rs77898819
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=) rs118175551
NM_001083961.2(WDR62):c.3231C>T (p.Pro1077=) rs187029707
NM_001083961.2(WDR62):c.3401T>G (p.Met1134Arg) rs61741470
NM_001083961.2(WDR62):c.3468C>T (p.Leu1156=) rs17851502
NM_001083961.2(WDR62):c.3639C>T (p.Ser1213=) rs45470992
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) rs61743589
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) rs2074435
NM_001083961.2(WDR62):c.4123G>A (p.Gly1375Ser) rs17851503
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe) rs1008328
NM_001083961.2(WDR62):c.562-13C>T rs78138007
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) rs12327568

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