List of variants in gene BCORL1 reported as benign by GeneDx

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_001379451.1(BCORL1):c.3396C>G (p.Leu1132=)	rs7062200	0.09421
NM_001379451.1(BCORL1):c.625G>A (p.Gly209Ser)	rs5932715	0.06906
NM_001379451.1(BCORL1):c.3189C>T (p.Ala1063=)	rs7061871	0.04949

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