List of variants in gene AFF2 reported as benign for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002025.4(AFF2):c.3404+7A>G	rs5980615	0.95464
NM_002025.4(AFF2):c.3623+57G>A	rs12688573	0.56066
NM_002025.4(AFF2):c.1041+56456A>G	rs241084	0.33601
NM_002025.4(AFF2):c.1488G>A (p.Ser496=)	rs12011040	0.14855
NM_002025.4(AFF2):c.1653A>G (p.Thr551=)	rs16994869	0.02513
NM_002025.4(AFF2):c.3837G>A (p.Thr1279=)	rs61743576	0.01510
NM_002025.4(AFF2):c.1353C>G (p.Leu451=)	rs138980868	0.00324
NM_002025.4(AFF2):c.3696A>T (p.Pro1232=)	rs35967616	0.00126
NM_002025.4(AFF2):c.1788C>A (p.Ala596=)	rs149492076	0.00109
NM_002025.4(AFF2):c.2780G>A (p.Arg927His)	rs140927355	0.00036
NM_002025.4(AFF2):c.1121C>A (p.Ser374Tyr)	rs200306870	0.00025
NM_002025.4(AFF2):c.2196C>T (p.Val732=)	rs202015083	0.00006
NM_002025.4(AFF2):c.1558-78G>C	rs16994868
NM_002025.4(AFF2):c.2181C>T (p.Thr727=)	rs143927826

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