Variants in gene RB1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.2212-16T>A	rs201258424	0.01386
NM_000321.3(RB1):c.411A>T (p.Glu137Asp)	rs3092902	0.00040
NM_000321.3(RB1):c.929G>A (p.Gly310Glu)	rs200844292	0.00029
NM_000321.3(RB1):c.-69G>C	rs753117180	0.00014
NM_000321.3(RB1):c.2360G>A (p.Arg787Gln)	rs748094394	0.00006
NM_000321.3(RB1):c.2003G>A (p.Arg668His)	rs551747882	0.00005
NM_000321.3(RB1):c.462G>A (p.Lys154=)	rs369830657	0.00004
NM_000321.3(RB1):c.731T>C (p.Ile244Thr)	rs147754935	0.00004
NM_000321.3(RB1):c.1859C>T (p.Thr620Met)	rs554834063	0.00003
NM_000321.3(RB1):c.1139A>G (p.Asn380Ser)	rs1470523018	0.00001
NM_000321.3(RB1):c.2393G>A (p.Arg798Gln)	rs374523971	0.00001
NM_000321.3(RB1):c.1861C>A (p.Arg621Ser)	rs367578442
NM_000321.3(RB1):c.397A>C (p.Asn133His)	rs3092900

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