List of variants in gene RET reported as uncertain significance by GeneKor MSA

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.785T>C (p.Val262Ala)	rs139790943	0.00024
NM_020975.6(RET):c.2657G>A (p.Arg886Gln)	rs373594744	0.00009
NM_020975.6(RET):c.1894G>A (p.Glu632Lys)	rs377767407	0.00006
NM_020975.6(RET):c.134C>T (p.Ala45Val)	rs763526874	0.00002
NM_020975.6(RET):c.1102C>T (p.Arg368Cys)	rs754116867	0.00001
NM_020975.6(RET):c.2080C>T (p.Arg694Trp)	rs193922700	0.00001
NM_020975.6(RET):c.2129A>G (p.Lys710Arg)	rs774983492	0.00001
NM_020975.6(RET):c.2162G>A (p.Arg721Gln)	rs1356141763	0.00001
NM_020975.6(RET):c.1487C>T (p.Ala496Val)	rs1356271817
NM_020975.6(RET):c.182A>C (p.Glu61Ala)	rs1564489398
NM_020975.6(RET):c.3079C>G (p.Leu1027Val)	rs1564501868
NM_020975.6(RET):c.765G>T (p.Met255Ile)	rs1564491302

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.