List of variants in gene AFF2 reported as likely benign 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002025.4(AFF2):c.3404+7A>G	rs5980615	0.95464
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.1788C>A (p.Ala596=)	rs149492076	0.00109
NM_002025.4(AFF2):c.3696A>T (p.Pro1232=)	rs35967616	0.00105
NM_002025.4(AFF2):c.496C>T (p.Pro166Ser)	rs150996735	0.00088
NM_002025.4(AFF2):c.2780G>A (p.Arg927His)	rs140927355	0.00036
NM_002025.4(AFF2):c.47+16T>C	rs782673472	0.00008
NM_002025.4(AFF2):c.2427A>G (p.Leu809=)	rs782571214	0.00002
NM_002025.4(AFF2):c.3138G>A (p.Ala1046=)	rs974621684	0.00001
NM_002025.4(AFF2):c.1034C>T (p.Thr345Ile)	rs199510763

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