List of variants in gene BNC2 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017637.6(BNC2):c.167C>G (p.Thr56Arg)	rs146566771	0.00276
NM_017637.6(BNC2):c.2789A>G (p.Asp930Gly)	rs41268965	0.00269
NM_017637.6(BNC2):c.1002A>G (p.Pro334=)	rs483353010

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