ClinVar Miner

List of variants in gene WDR62 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_001083961.2(WDR62):c.1233+220C>T
NM_001083961.2(WDR62):c.1371+92T>C
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) rs62109744
NM_001083961.2(WDR62):c.1550+218A>G
NM_001083961.2(WDR62):c.1643-39G>A rs2301735
NM_001083961.2(WDR62):c.1768+220G>A
NM_001083961.2(WDR62):c.1768+28G>A rs77938609
NM_001083961.2(WDR62):c.177+177C>G
NM_001083961.2(WDR62):c.1959-84G>C
NM_001083961.2(WDR62):c.2035-115T>C
NM_001083961.2(WDR62):c.2035-125C>T
NM_001083961.2(WDR62):c.2147-34G>A rs2301736
NM_001083961.2(WDR62):c.2210+280C>T
NM_001083961.2(WDR62):c.2210+301C>G
NM_001083961.2(WDR62):c.2211-168del
NM_001083961.2(WDR62):c.2312A>G (p.Lys771Arg) rs61747277
NM_001083961.2(WDR62):c.2334-152G>A
NM_001083961.2(WDR62):c.2334-29C>T rs2301737
NM_001083961.2(WDR62):c.2334-331C>T
NM_001083961.2(WDR62):c.2334-6C>A rs138928852
NM_001083961.2(WDR62):c.2467+108G>A
NM_001083961.2(WDR62):c.2467+46_2467+47del
NM_001083961.2(WDR62):c.2521-133G>A
NM_001083961.2(WDR62):c.2521-140C>T
NM_001083961.2(WDR62):c.2549T>C (p.Leu850Ser) rs2285745
NM_001083961.2(WDR62):c.2739+173G>A
NM_001083961.2(WDR62):c.2740-219G>C
NM_001083961.2(WDR62):c.2740-234A>G
NM_001083961.2(WDR62):c.2971+138C>T
NM_001083961.2(WDR62):c.3082+76G>T
NM_001083961.2(WDR62):c.3514+44G>A rs45468494
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) rs61743589
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) rs111294536
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) rs2074435
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) rs35811023
NM_001083961.2(WDR62):c.4153+153G>T
NM_001083961.2(WDR62):c.4154-162G>C
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe) rs1008328
NM_001083961.2(WDR62):c.562-324G>C
NM_001083961.2(WDR62):c.562-335G>A
NM_001083961.2(WDR62):c.562-95T>C
NM_001083961.2(WDR62):c.883-166G>A

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.