List of variants reported as pathogenic for hereditary retinoblastoma by Genetics Program, Instituto Nacional de Cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.1215+1G>A	rs587776783
NM_000321.3(RB1):c.1498+2T>G	rs1948523741
NM_000321.3(RB1):c.1901C>G (p.Ser634Ter)	rs1949359603
NM_000321.3(RB1):c.1960+1G>T	rs1949360306
NM_000321.3(RB1):c.2035_2038dup (p.Ile680fs)	rs1949384403
NM_000321.3(RB1):c.380+1G>A	rs1131690902
NM_000321.3(RB1):c.763C>T (p.Arg255Ter)	rs587778842

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.