ClinVar Miner

List of variants reported as likely benign for RIN2 syndrome

Included ClinVar conditions (1):

Macrocephaly, alopecia, cutis laxa, and scoliosis

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

Total variants: 1

Download table as spreadsheet

HGVS	dbSNP
NM_018993.3(RIN2):c.1642G>A (p.Val548Met)	rs181298473

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.