List of variants in gene ARID1A reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_006015.6(ARID1A):c.6586C>T (p.Leu2196=)	rs149633292	0.00468
NM_006015.6(ARID1A):c.5001G>A (p.Pro1667=)	rs116540923	0.00363
NM_006015.6(ARID1A):c.2541C>A (p.Ile847=)	rs151274586	0.00329
NM_006015.6(ARID1A):c.318C>T (p.Asn106=)	rs551186176	0.00196
NM_006015.6(ARID1A):c.5336A>G (p.Glu1779Gly)	rs140946580	0.00112
NM_006015.6(ARID1A):c.472C>T (p.Pro158Ser)	rs567246585	0.00088
NM_006015.6(ARID1A):c.3762C>T (p.Gly1254=)	rs138814830	0.00060
NM_006015.6(ARID1A):c.5076C>T (p.Asn1692=)	rs149468118	0.00038
NM_006015.6(ARID1A):c.4053C>T (p.Gly1351=)	rs200122106	0.00031
NM_006015.6(ARID1A):c.6659A>G (p.Asn2220Ser)	rs139576809	0.00029
NM_006015.6(ARID1A):c.3978GCA[9] (p.Gln1334dup)	rs374564889
NM_006015.6(ARID1A):c.4538G>A (p.Ser1513Asn)	rs2124120299
NM_006015.6(ARID1A):c.4927C>A (p.Pro1643Thr)	rs1454897845
NM_006015.6(ARID1A):c.5438C>T (p.Pro1813Leu)	rs1373371414
NM_006015.6(ARID1A):c.5717G>A (p.Arg1906Gln)	rs41303631

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