List of variants in gene LOC106736614, RET studied for benign neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020630.5(RET):c.-200A>G	rs10900296	0.77447
NM_020975.5(RET):c.-196C>A	rs10900297	0.41632
NM_020975.6(RET):c.-132G>T	rs886046985	0.00103
NM_020975.6(RET):c.-2C>A	rs876657980	0.00049
NM_020975.6(RET):c.-51C>T	rs765384640	0.00012
NM_020975.6(RET):c.-158G>A	rs886046984	0.00001
NM_020975.6(RET):c.-160G>T	rs567112195
NM_020975.6(RET):c.-173A>G	rs1359755826
NM_020975.6(RET):c.-187C>A	rs886046983
NM_020975.6(RET):c.20G>A (p.Gly7Asp)	rs1366681125
NM_020975.6(RET):c.31C>T (p.Leu11=)	rs587780812

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.