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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe)	rs1008328	0.75234
NM_001083961.2(WDR62):c.2549T>C (p.Leu850Ser)	rs2285745	0.68524
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu)	rs2074435	0.67816
NM_001083961.2(WDR62):c.186C>T (p.Leu62=)	rs11538454	0.14792
NM_001083961.2(WDR62):c.3468C>T (p.Leu1156=)	rs17851502	0.14024
NM_001083961.2(WDR62):c.2271G>A (p.Leu757=)	rs61494900	0.13796
NM_001083961.2(WDR62):c.1643-10C>T	rs4806263	0.13606
NM_001083961.2(WDR62):c.1470C>T (p.Asp490=)	rs45567532	0.13368
NM_001083961.2(WDR62):c.180G>A (p.Val60=)	rs61742664	0.04980
NM_001083961.2(WDR62):c.562-13C>T	rs78138007	0.03579
NM_001083961.2(WDR62):c.4123G>A (p.Gly1375Ser)	rs17851503	0.03516
NM_001083961.2(WDR62):c.3401T>G (p.Met1134Arg)	rs61741470	0.03313
NM_001083961.2(WDR62):c.3639C>T (p.Ser1213=)	rs45470992	0.03266
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His)	rs61743589	0.02069
NM_001083961.2(WDR62):c.2312A>G (p.Lys771Arg)	rs61747277	0.01994
NM_001083961.2(WDR62):c.2281C>T (p.His761Tyr)	rs61744321	0.01766
NM_001083961.2(WDR62):c.1642+8C>T	rs143309981	0.01050
NM_001083961.2(WDR62):c.2975C>T (p.Ser992Leu)	rs74518295	0.00953
NM_001083961.2(WDR62):c.2991C>T (p.Ala997=)	rs77898819	0.00804
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe)	rs62109744	0.00795
NM_001083961.2(WDR62):c.2334-6C>A	rs138928852	0.00461
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg)	rs12327568	0.00459
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp)	rs146180912	0.00414
NM_001083961.2(WDR62):c.1233+13C>T	rs76130844
NM_001083961.2(WDR62):c.1315T>G (p.Phe439Val)	rs75230537
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=)	rs2301734
NM_001083961.2(WDR62):c.186C>G (p.Leu62=)	rs11538454
NM_001083961.2(WDR62):c.269+12del	rs797046108

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