List of variants in gene RB1 reported as likely benign by Mendelics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.2521-11G>A	rs4151624	0.00570
NM_000321.3(RB1):c.2490-45A>G	rs4151610	0.00540
NM_000321.3(RB1):c.380+10C>G	rs187110786	0.00158
NM_000321.3(RB1):c.1129A>T (p.Thr377Ser)	rs146897002	0.00080
NM_000321.3(RB1):c.929G>A (p.Gly310Glu)	rs200844292	0.00029
NM_000321.3(RB1):c.113G>A (p.Gly38Asp)	rs766529534	0.00016
NM_000321.3(RB1):c.1156A>G (p.Met386Val)	rs564780653	0.00014
NM_000321.3(RB1):c.2521-4G>T	rs902298592

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