List of variants in gene RARB reported as uncertain significance for Inborn genetic diseases

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

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000965.5(RARB):c.148A>G (p.Thr50Ala)	rs1057524213	0.00001
NM_000965.5(RARB):c.356G>A (p.Arg119Gln)	rs1292531557	0.00001
NM_000965.5(RARB):c.1097T>C (p.Met366Thr)	rs781234532
NM_000965.5(RARB):c.1298C>G (p.Pro433Arg)
NM_000965.5(RARB):c.40C>G (p.Gln14Glu)
NM_000965.5(RARB):c.646G>A (p.Gly216Ser)	rs373578752
NM_000965.5(RARB):c.737C>G (p.Thr246Ser)	rs1248468594
NM_000965.5(RARB):c.845G>T (p.Gly282Val)	rs2529811664
NM_000965.5(RARB):c.961C>A (p.Leu321Ile)	rs1436425031

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.