List of variants in gene RB1 reported as benign for not specified

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.500+23T>G	rs198617	0.93273
NM_000321.3(RB1):c.2663+33C>T	rs3020646	0.90292
NM_000321.3(RB1):c.380+45C>T	rs520342	0.21231
NM_000321.3(RB1):c.2664-10T>A	rs3092904	0.19833
NM_000321.3(RB1):c.1390-14A>T	rs9535023	0.04866
NM_000321.3(RB1):c.1216-29A>G	rs3092886	0.02593
NM_000321.3(RB1):c.2490-1323C>T	rs55926808	0.01180
NM_000321.3(RB1):c.380+12T>C	rs3092881	0.01087
NM_000321.3(RB1):c.2521-11G>A	rs4151624	0.00570
NM_000321.3(RB1):c.1390-11A>G	rs200658795	0.00365
NM_000321.3(RB1):c.2212-6C>T	rs776162179	0.00164
NM_000321.3(RB1):c.380+10C>G	rs187110786	0.00158
NM_000321.3(RB1):c.1961-12T>C	rs201697122	0.00104
NM_000321.3(RB1):c.920C>T (p.Thr307Ile)	rs183898408	0.00079
NM_000321.3(RB1):c.1770T>C (p.Cys590=)	rs145310579	0.00062
NM_000321.3(RB1):c.1390-17dup	rs753535084
NM_000321.3(RB1):c.1422-8del	rs747048469
NM_000321.3(RB1):c.1499-10del	rs148580581
NM_000321.3(RB1):c.2212-16del
NM_000321.3(RB1):c.2212-16dup	rs553094345
NM_000321.3(RB1):c.2212-9C>A	rs765386327
NM_000321.3(RB1):c.45_53del (p.Ala16_Ala18del)	rs572454921
NM_000321.3(RB1):c.608-4del	rs762805947

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