List of variants in gene combination LOC129935846, PDE6D reported as likely 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002601.4(PDE6D):c.33C>T (p.Ile11=)	rs769953849	0.00001
NM_002601.4(PDE6D):c.15C>T (p.Asp5=)	rs2106294236
NM_002601.4(PDE6D):c.6A>C (p.Ser2=)

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