List of variants in gene RYR3 reported as likely benign for not specified

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001036.6(RYR3):c.4296C>T (p.Gly1432=)	rs61749016	0.00086
NM_001036.6(RYR3):c.1373G>A (p.Arg458Gln)	rs74005691	0.00083
NM_001036.6(RYR3):c.280-12T>C	rs375322559	0.00054
NM_001036.6(RYR3):c.13584A>G (p.Glu4528=)	rs200841538	0.00040
NM_001036.6(RYR3):c.12463G>A (p.Asp4155Asn)	rs200893645	0.00009
NM_001036.6(RYR3):c.8137-3T>C	rs141534340	0.00008
NM_001036.6(RYR3):c.6025A>G (p.Thr2009Ala)	rs888626789	0.00005
NM_001036.6(RYR3):c.3334G>A (p.Val1112Ile)	rs757239023	0.00004
NM_001036.6(RYR3):c.5356G>A (p.Gly1786Ser)	rs759581452	0.00001
NM_001036.6(RYR3):c.5591A>G (p.Lys1864Arg)	rs774589130	0.00001
NM_001036.6(RYR3):c.12595C>T (p.Leu4199Phe)
NM_001036.6(RYR3):c.12959A>G (p.Gln4320Arg)
NM_001036.6(RYR3):c.2560G>A (p.Val854Ile)
NM_001036.6(RYR3):c.78C>T (p.Ile26=)	rs199968653
NM_001036.6(RYR3):c.8154T>G (p.Pro2718=)
NM_001036.6(RYR3):c.9143G>T (p.Arg3048Leu)	rs139568967

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.