List of variants in gene AFF2 reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002025.4(AFF2):c.3088A>C (p.Ile1030Leu)	rs149653283	0.00046
NM_002025.4(AFF2):c.561C>A (p.Asp187Glu)	rs201152809	0.00014
NM_002025.4(AFF2):c.3589G>A (p.Ala1197Thr)	rs373659849	0.00013
NM_002025.4(AFF2):c.1541G>C (p.Arg514Pro)	rs369100046	0.00005
NM_002025.4(AFF2):c.733G>A (p.Ala245Thr)	rs147842224	0.00005
NM_002025.4(AFF2):c.1830G>C (p.Leu610Phe)	rs200450195	0.00003
NM_002025.4(AFF2):c.1118C>G (p.Thr373Ser)	rs587780276
NM_002025.4(AFF2):c.1133C>G (p.Ala378Gly)	rs797045218
NM_002025.4(AFF2):c.2702C>A (p.Ser901Tyr)	rs782757734
NM_002025.4(AFF2):c.292C>A (p.Pro98Thr)	rs797045219
NM_002025.4(AFF2):c.3081C>T (p.Thr1027=)	rs797045220
NM_002025.4(AFF2):c.3697G>A (p.Val1233Ile)	rs1557291713

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