List of variants in gene combination ARID1B, LOC115308161 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001374828.1(ARID1B):c.347C>T (p.Ala116Val)	rs1325414473	0.00001
NM_001374828.1(ARID1B):c.352TCC[6] (p.Ser124del)	rs770512547
NM_001374828.1(ARID1B):c.537_560del (p.His181_Ala188del)	rs1554247278

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