ClinVar Miner

List of variants in gene FLVCR2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017791.3(FLVCR2):c.670-16394T>C rs4903337 0.43340
NM_017791.3(FLVCR2):c.648C>G (p.Ser216=) rs2287017 0.37676
NM_017791.3(FLVCR2):c.47T>C (p.Val16Ala) rs2287015 0.37478
NM_017791.3(FLVCR2):c.-96T>C rs11845734 0.36446
NM_017791.3(FLVCR2):c.670-16728C>T rs3784006 0.19084
NM_017791.3(FLVCR2):c.376C>T (p.Leu126=) rs8011292 0.17455
NM_017791.2(FLVCR2):c.-356G>C rs3813550 0.11387
NM_017791.3(FLVCR2):c.1124+30T>C rs12436885 0.08775
NM_017791.3(FLVCR2):c.-71C>T rs11849590 0.08516
NM_017791.3(FLVCR2):c.952+102T>G rs117232115 0.05545
NM_017791.3(FLVCR2):c.812-264G>A rs111569748 0.05355
NM_017791.3(FLVCR2):c.1509+181C>T rs2302591 0.04743
NM_017791.3(FLVCR2):c.1341+52G>A rs111451537 0.04204
NM_017791.3(FLVCR2):c.669+160G>A rs11850801 0.03322
NM_017791.3(FLVCR2):c.1021-269A>C rs28453294 0.02262
NM_017791.3(FLVCR2):c.1453+41C>T rs74067119 0.02072
NM_017791.3(FLVCR2):c.1441G>A (p.Ala481Thr) rs35126362 0.01730
NM_017791.3(FLVCR2):c.670-16207G>T rs116091794 0.01516
NM_017791.3(FLVCR2):c.670-191G>A rs77304161 0.01510
NM_017791.3(FLVCR2):c.1124+36A>G rs79451870 0.00214
NM_017791.3(FLVCR2):c.-121CT[1] rs1322268460
NM_017791.3(FLVCR2):c.1509+182G>T rs12323563
NM_017791.3(FLVCR2):c.543G>A (p.Val181=) rs2287016
NM_017791.3(FLVCR2):c.669+246C>T rs17103483

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.