List of variants in gene RET reported as benign by Athena Diagnostics Inc

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.135= (p.Ala45=)	rs1800858	0.20726
NM_020975.6(RET):c.2307= (p.Leu769=)	rs1800861	0.20453
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.868-18G>A	rs57098408	0.01028
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.2226G>A (p.Thr742=)	rs762876946	0.00002

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.