List of variants in gene ARID1B reported as uncertain significance 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.1170CGG[4] (p.Gly399_Gly402del)	rs587779747
NM_001374828.1(ARID1B):c.1292CAG[4] (p.Ala433_Gly434insAla)	rs797045267
NM_001374828.1(ARID1B):c.1303GGC[7] (p.Gly440_Tyr441insGly)	rs797045268

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