List of variants in gene BIN1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.1003-15G>A	rs149290511	0.00095
NM_139343.3(BIN1):c.402C>T (p.Pro134=)	rs144136512	0.00023
NM_139343.3(BIN1):c.1143G>A (p.Pro381=)	rs372360787	0.00018
NM_139343.3(BIN1):c.316-19G>A	rs369840788	0.00018
NM_139343.3(BIN1):c.699-13C>T	rs373662459	0.00011
NM_139343.3(BIN1):c.285C>T (p.Pro95=)	rs377467117	0.00008
NM_139343.3(BIN1):c.1587C>T (p.His529=)	rs144458131	0.00007
NM_139343.3(BIN1):c.858-1472C>G	rs185803812	0.00006
NM_139343.3(BIN1):c.675G>A (p.Glu225=)	rs148179522	0.00003
NM_139343.3(BIN1):c.1264-8G>A	rs776696908	0.00002
NM_139343.3(BIN1):c.1132-22TGC[5]
NM_139343.3(BIN1):c.1674+7G>C
NM_139343.3(BIN1):c.177C>G (p.Thr59=)
NM_139343.3(BIN1):c.342C>T (p.Tyr114=)
NM_139343.3(BIN1):c.630C>T (p.Ile210=)	rs886038728

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