ClinVar Miner

List of variants in gene RD3 reported as uncertain significance for Leber congenital amaurosis

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
NM_001164688.1(RD3):c.-166_-165GA[1] rs886045903
NM_001164688.1(RD3):c.-336_-335AC[16] rs34485370
NM_001164688.1(RD3):c.-336_-335AC[19] rs34485370
NM_001164688.1(RD3):c.-336_-335AC[20] rs34485370
NM_001164688.1(RD3):c.-336_-335AC[21] rs34485370
NM_001164688.1(RD3):c.-336_-335AC[23] rs34485370
NM_001164688.1(RD3):c.-336_-335AC[24] rs34485370
NM_183059.2(RD3):c.*1305del rs886045896
NM_183059.2(RD3):c.*1582del rs879756831
NM_183059.2(RD3):c.*1582dup rs879756831
NM_183059.2(RD3):c.*1583del rs775682217
NM_183059.2(RD3):c.-295_-294del rs1553282313
NM_183059.2(RD3):c.-296_-295dup rs1491560139
NM_183059.2(RD3):c.-305_-297delinsC rs886045910
NM_183059.2(RD3):c.-307_-297delinsC rs886045911
NM_183059.2(RD3):c.-340_-339del rs886045915
NM_183059.2(RD3):c.-343_-340del rs886045916

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.