List of variants reported as benign for Joubert syndrome 8

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001174150.2(ARL13B):c.1043C>G (p.Thr348Ser)	rs33944211	0.07857
NM_001174150.2(ARL13B):c.105C>T (p.Thr35=)	rs146396078	0.00721
NM_001174150.2(ARL13B):c.1186C>G (p.Pro396Ala)	rs11554412	0.00529
NM_001174150.2(ARL13B):c.689+19T>C	rs376881421	0.00078
NM_001174150.2(ARL13B):c.1032T>C (p.Gly344=)	rs561410801	0.00020
NM_001174150.2(ARL13B):c.568A>G (p.Ile190Val)	rs193219215	0.00011
NM_001174150.2(ARL13B):c.671G>A (p.Arg224Gln)	rs542323478	0.00001
NM_001174150.2(ARL13B):c.422C>G (p.Ala141Gly)	rs529580146
NM_001174150.2(ARL13B):c.486+22del	rs368491848
NM_001174150.2(ARL13B):c.59+20C>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.