List of variants in gene PDE6B reported as likely benign by GeneDx

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000283.4(PDE6B):c.469-179C>T	rs34391278	0.02959
NM_000283.4(PDE6B):c.1401+110A>G	rs530816505	0.02455
NM_000283.4(PDE6B):c.2504-205G>C	rs35925646	0.02197
NM_000283.4(PDE6B):c.1467+41C>T	rs116283697	0.02034
NM_000283.4(PDE6B):c.621+194G>A	rs1212960611	0.01359
NM_000283.4(PDE6B):c.2289G>A (p.Lys763=)	rs61739716	0.01153
NM_000283.4(PDE6B):c.928-175G>A	rs116353162	0.00847
NM_000283.4(PDE6B):c.655T>C (p.Tyr219His)	rs62295357	0.00465
NM_000283.4(PDE6B):c.1108-10G>A	rs374534089	0.00018
NM_000283.4(PDE6B):c.1401+110_1401+155del
NM_000283.4(PDE6B):c.1832+237_1832+238del	rs36093261
NM_000283.4(PDE6B):c.1833-53G>T
NM_000283.4(PDE6B):c.2268+26A>T	rs76590730
NM_000283.4(PDE6B):c.993-49G>C	rs115328178

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