List of variants in gene ARL13B reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001174150.2(ARL13B):c.1043C>G (p.Thr348Ser)	rs33944211	0.08150
NM_001174150.2(ARL13B):c.1186C>G (p.Pro396Ala)	rs11554412	0.00529
NM_001174150.2(ARL13B):c.130+7T>C	rs200527262	0.00047

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