List of variants in gene ARID1B reported as benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_001374828.1(ARID1B):c.2629C>T (p.Pro877Ser)	rs114201726	0.00727
NM_001374828.1(ARID1B):c.3106G>A (p.Gly1036Ser)	rs34786733	0.00590
NM_001374828.1(ARID1B):c.985G>A (p.Gly329Ser)	rs375160616	0.00475

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