ClinVar Miner

List of variants in gene FREM1 reported by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001379081.2(FREM1):c.4945A>G (p.Ile1649Val) rs199891537 0.00030
NM_001379081.2(FREM1):c.4552G>T (p.Ala1518Ser) rs775792241 0.00009
NM_001379081.2(FREM1):c.5186A>G (p.Asn1729Ser) rs1211552660 0.00001
NM_001379081.2(FREM1):c.6037T>A (p.Cys2013Ser) rs1420458990 0.00001
NM_001379081.2(FREM1):c.4064A>C (p.His1355Pro) rs763901210
NM_001379081.2(FREM1):c.4204C>G (p.Leu1402Val) rs770679670
NM_001379081.2(FREM1):c.617T>C (p.Phe206Ser) rs2131557195

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.