List of variants in gene WDR62 reported as benign by Eurofins NTD LLC (GA)

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe)	rs1008328	0.75234
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu)	rs2074435	0.67813
NM_001083961.2(WDR62):c.180G>A (p.Val60=)	rs61742664	0.04216
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.*5G>A	rs61740165	0.00745
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu)	rs35811023	0.00416
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=)	rs149289227	0.00183
NM_001083961.2(WDR62):c.2016C>T (p.Asp672=)	rs114968951	0.00170
NM_001083961.2(WDR62):c.3231C>T (p.Pro1077=)	rs187029707	0.00102
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=)	rs144697999	0.00073
NM_001083961.2(WDR62):c.1233+15dup	rs373693641
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=)	rs2301734
NM_001083961.2(WDR62):c.2112G>C (p.Ser704=)	rs115453534
NM_001083961.2(WDR62):c.3271_3273del (p.His1091del)	rs794727435

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.