ClinVar Miner

List of variants in gene RFWD3 reported as uncertain significance for Fanconi anemia, complementation group W

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018124.4(RFWD3):c.1367G>C (p.Cys456Ser) rs773701779 0.00001
NM_018124.4(RFWD3):c.1189G>C (p.Val397Leu) rs1567572985
NM_018124.4(RFWD3):c.1577G>A (p.Ser526Asn)

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.