List of variants in gene BIN1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.486T>C (p.Thr162=)	rs1060743	0.29063
NM_139343.3(BIN1):c.957C>T (p.Ala319=)	rs2276579	0.13837
NM_139343.3(BIN1):c.894G>A (p.Ser298=)	rs2228955	0.03955
NM_139343.3(BIN1):c.1595C>T (p.Thr532Met)	rs112318500	0.03069
NM_139343.3(BIN1):c.1263+11C>T	rs78967885	0.00935
NM_139343.3(BIN1):c.1132-7T>C	rs115938552	0.00498
NM_139343.3(BIN1):c.888C>T (p.Ser296=)	rs114833236	0.00403
NM_139343.3(BIN1):c.696C>A (p.Asn232Lys)	rs143820618	0.00034
NM_139343.3(BIN1):c.1710C>T (p.Asp570=)	rs587783342

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