List of variants in gene KITLG reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000899.5(KITLG):c.213C>T (p.Ser71=)	rs17015782	0.01140
NM_000899.5(KITLG):c.628G>T (p.Asp210Tyr)	rs41283112	0.01027
NM_000899.5(KITLG):c.177C>T (p.Pro59=)	rs61924705	0.00192
NM_000899.5(KITLG):c.255G>C (p.Leu85=)	rs767292529	0.00001
NM_000899.5(KITLG):c.708C>T (p.Tyr236=)	rs200147285	0.00001
NM_000899.5(KITLG):c.130-11dup	rs11428619
NM_000899.5(KITLG):c.15+2T>A	rs1592593751

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.