List of variants in gene combination CEP104, LOC126805587 reported as benign for Joubert syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014704.4(CEP104):c.1836+7A>G	rs6413779	0.90433
NM_014704.4(CEP104):c.1836+14G>A	rs75027831	0.00632

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