List of variants in gene BBS9 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_198428.3(BBS9):c.1646C>T (p.Thr549Ile)	rs59252892	0.00979
NM_198428.3(BBS9):c.1993C>T (p.Leu665Phe)	rs116262072	0.00392
NM_198428.3(BBS9):c.2216C>T (p.Ala739Val)	rs116483694	0.00287
NM_198428.3(BBS9):c.2632+9C>A	rs148654647	0.00242
NM_198428.3(BBS9):c.1648A>G (p.Ile550Val)	rs150399299	0.00219
NM_198428.3(BBS9):c.2646C>A (p.Leu882=)	rs61753527	0.00088
NM_198428.3(BBS9):c.2363C>T (p.Ser788Phe)	rs61753526	0.00053
NM_198428.3(BBS9):c.2322C>T (p.Ala774=)	rs145435891	0.00037
NM_198428.3(BBS9):c.621C>T (p.Tyr207=)	rs140169161	0.00026
NM_198428.3(BBS9):c.771A>G (p.Ala257=)	rs145007686	0.00021
NM_198428.3(BBS9):c.270C>T (p.Thr90=)	rs747398844	0.00005
NM_198428.3(BBS9):c.2139G>A (p.Val713=)	rs1554512125
NM_198428.3(BBS9):c.2499C>T (p.Ala833=)	rs1163398668
NM_198428.3(BBS9):c.528T>G (p.Pro176=)	rs757308943

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