List of variants in gene AFF4 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014423.4(AFF4):c.819G>A (p.Glu273=)	rs141383886	0.00480
NM_014423.4(AFF4):c.3319A>G (p.Thr1107Ala)	rs139490054	0.00217
NM_014423.4(AFF4):c.830G>C (p.Ser277Thr)	rs141068875	0.00073

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