List of variants in gene ARID2 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_152641.4(ARID2):c.638-40G>A	rs2059404	0.47840
NM_152641.4(ARID2):c.419-57T>C	rs17774927	0.15034
NM_152641.4(ARID2):c.3171G>A (p.Ser1057=)	rs7296694	0.09069
NM_152641.4(ARID2):c.4300G>T (p.Ala1434Ser)	rs150136669	0.00436
NM_152641.4(ARID2):c.5062-45A>G	rs373695302	0.00011
NM_152641.4(ARID2):c.-14C>G	rs375590924	0.00010
NM_152641.4(ARID2):c.284+32G>T	rs371802419	0.00010
NC_000012.12:g.45729667GCC[13]	rs71067904
NM_152641.4(ARID2):c.4774-83_4774-82del	rs10577231

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