List of variants in gene FREM2 reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_207361.6(FREM2):c.8885C>T (p.Ala2962Val)	rs7996253	0.02012
NM_207361.6(FREM2):c.3116T>A (p.Met1039Lys)	rs2496424	0.01608
NM_207361.6(FREM2):c.1188G>C (p.Gln396His)	rs61997174	0.00747
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile)	rs116099212	0.00379
NM_207361.6(FREM2):c.5810C>T (p.Ser1937Phe)	rs1020313300	0.00001

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.