List of variants in gene BIN1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.888C>T (p.Ser296=)	rs114833236	0.00403
NM_139343.3(BIN1):c.30G>A (p.Thr10=)	rs35535012	0.00067
NM_139343.3(BIN1):c.924C>T (p.Pro308=)	rs367611371	0.00005
NM_139343.3(BIN1):c.450C>T (p.Tyr150=)	rs550177667	0.00003
NM_139343.3(BIN1):c.393C>T (p.Gly131=)	rs1455926606	0.00002
NM_139343.3(BIN1):c.1017A>C (p.Pro339=)
NM_139343.3(BIN1):c.1124C>G (p.Pro375Arg)	rs2104935838
NM_139343.3(BIN1):c.1227G>A (p.Thr409=)
NM_139343.3(BIN1):c.1515C>T (p.Thr505=)	rs375583449
NM_139343.3(BIN1):c.543C>T (p.Ala181=)

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