ClinVar Miner

List of variants in gene RB1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NC_000013.11:g.48360013del
NM_000321.2(RB1):c.1216-29A>G rs3092886
NM_000321.2(RB1):c.1218C>T (p.Asn406=)
NM_000321.2(RB1):c.1814+11T>C
NM_000321.2(RB1):c.570G>A (p.Val190=) rs775061547
NM_000321.2:c.2714-10C>T

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.