List of variants in gene combination BCOR, LOC126863239 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001123385.2(BCOR):c.1260T>C (p.Asp420=)	rs5917933	0.91469
NM_001123385.2(BCOR):c.409G>A (p.Val137Ile)	rs146403660	0.00042
NM_001123385.2(BCOR):c.696G>A (p.Pro232=)	rs752884103	0.00003
NM_001123385.2(BCOR):c.790C>T (p.Pro264Ser)	rs1935688006

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