Variants in gene BIN1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.1263+11C>T	rs78967885	0.00935
NM_139343.3(BIN1):c.1625A>G (p.Lys542Arg)	rs138047593	0.00841
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.384G>A (p.Thr128=)	rs61748158	0.00203
NM_139343.3(BIN1):c.30G>A (p.Thr10=)	rs35535012	0.00067
NM_139343.3(BIN1):c.1131+9C>T	rs138606879	0.00005
NM_139343.3(BIN1):c.1132-22TGC[7]	rs748026377

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