ClinVar Miner

List of variants in gene FREM2 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.*3731A>C rs41286133 0.01007
NM_207361.6(FREM2):c.*4907C>T rs185608262 0.00754
NM_207361.6(FREM2):c.4031G>A (p.Arg1344His) rs143044921 0.00430
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile) rs116099212 0.00379
NM_207361.6(FREM2):c.4319C>A (p.Thr1440Lys) rs79048205 0.00348
NM_207361.6(FREM2):c.84C>G (p.Pro28=) rs141718695 0.00194
NM_207361.6(FREM2):c.7323G>A (p.Ala2441=) rs147563277 0.00155
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met) rs114400765 0.00118
NM_207361.6(FREM2):c.1737C>T (p.Ile579=) rs144811771 0.00012
NM_207361.6(FREM2):c.6465T>C (p.Asp2155=) rs373878188 0.00005
NM_207361.6(FREM2):c.1250T>C (p.Leu417Pro) rs571694324 0.00003
NM_207361.6(FREM2):c.3629C>T (p.Thr1210Ile)
NM_207361.6(FREM2):c.3677C>G (p.Thr1226Ser)
NM_207361.6(FREM2):c.3729A>C (p.Ile1243=) rs1306457101
NM_207361.6(FREM2):c.3937G>T (p.Glu1313Ter) rs759421771
NM_207361.6(FREM2):c.4350C>A (p.Asn1450Lys) rs1869872750
NM_207361.6(FREM2):c.4688C>T (p.Thr1563Ile) rs772941769
NM_207361.6(FREM2):c.7209T>C (p.Cys2403=)

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.