Variants in gene PDE6B with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_000283.4(PDE6B):c.811G>A (p.Glu271Lys)	rs374156343	0.00006
NM_000283.4(PDE6B):c.1685G>A (p.Gly562Asp)	rs774268095	0.00004
NM_000283.4(PDE6B):c.299G>A (p.Arg100His)	rs555600300	0.00003
NM_000283.4(PDE6B):c.1920+2T>C	rs763996159	0.00001
NM_000283.4(PDE6B):c.409G>A (p.Gly137Arg)	rs781658083	0.00001
NM_000283.4(PDE6B):c.2152G>A (p.Asp718Asn)	rs150639487
NM_000283.4(PDE6B):c.2429T>C (p.Leu810Pro)	rs1737988951

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