ClinVar Miner

List of variants in gene FLAD1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025207.5(FLAD1):c.373-516G>A rs113906979 0.01194
NM_025207.5(FLAD1):c.372+186C>G rs78605724 0.01098
NM_025207.5(FLAD1):c.1555-235C>A rs114503518 0.01095
NM_025207.5(FLAD1):c.1118-163_1118-162del rs372031707 0.00448
NM_025207.5(FLAD1):c.1310G>A (p.Arg437His) rs144820916 0.00210
NM_025207.5(FLAD1):c.1118-33C>T rs191570212 0.00177
NM_025207.5(FLAD1):c.729C>T (p.Phe243=) rs61736264 0.00173
NM_025207.5(FLAD1):c.-27A>G rs373075625 0.00091
NM_025207.5(FLAD1):c.683G>A (p.Arg228His) rs144986636 0.00088
NM_025207.5(FLAD1):c.1119G>A (p.Gly373=) rs142224458 0.00083
NM_025207.5(FLAD1):c.640G>A (p.Gly214Arg) rs145054820 0.00074
NM_025207.5(FLAD1):c.1184G>A (p.Ser395Asn) rs146796757 0.00049
NM_025207.5(FLAD1):c.645A>G (p.Glu215=) rs138843652 0.00039
NM_025207.5(FLAD1):c.1566C>T (p.Tyr522=) rs148439225 0.00023
NM_025207.5(FLAD1):c.1555-19T>G rs369848433 0.00004
NM_025207.5(FLAD1):c.1555-10G>A rs1227440416 0.00003
NM_025207.5(FLAD1):c.-304C>T rs537748007 0.00001
NM_025207.5(FLAD1):c.1167C>T (p.Thr389=) rs368097196 0.00001
NM_025207.5(FLAD1):c.1212C>T (p.Asn404=) rs751432092 0.00001
NM_025207.5(FLAD1):c.-294AG[1] rs569007120

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.