List of variants in gene ARID1B reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001374828.1(ARID1B):c.6110G>A (p.Arg2037Gln)	rs751391187	0.00003
NM_001374828.1(ARID1B):c.1046T>G (p.Met349Arg)	rs1401971317	0.00002
NM_001374828.1(ARID1B):c.1987-10T>G	rs1276255111	0.00001
NM_001374828.1(ARID1B):c.4245C>G (p.Ser1415Arg)	rs1453138221
NM_001374828.1(ARID1B):c.4479G>A (p.Pro1493=)	rs797045277
NM_001374828.1(ARID1B):c.4894G>A (p.Glu1632Lys)	rs1340183572
NM_001374828.1(ARID1B):c.5092C>G (p.Leu1698Val)	rs1794104878
NM_001374828.1(ARID1B):c.6592G>T (p.Val2198Phe)	rs1794548648

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