List of variants in gene ARID1B reported as likely pathogenic by Laboratory of Molecular Genetics, CHU Rennes

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.3655_3656dup (p.Pro1220fs)	rs1057519009
NM_001374828.1(ARID1B):c.5394+1G>A	rs1057518984
NM_001374828.1(ARID1B):c.6726del (p.Asp2244fs)	rs1057519002

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