List of variants in gene CEP41 reported as uncertain significance for Joubert syndrome 1

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

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HGVS	dbSNP	gnomAD frequency
NM_018718.2(CEP41):c.-243G>A	rs542293061	0.00425
NM_018718.3(CEP41):c.*3741A>T	rs532169706	0.00076
NM_018718.3(CEP41):c.786G>A (p.Pro262=)	rs782460743	0.00005
NM_018718.2(CEP41):c.-178C>A	rs10230670
NM_018718.2(CEP41):c.-244A>T	rs886062003
NM_018718.3(CEP41):c.*1357del	rs886061999
NM_018718.3(CEP41):c.*1384del	rs55776575
NM_018718.3(CEP41):c.*1384dup	rs55776575
NM_018718.3(CEP41):c.*1386dup	rs886061997

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