List of variants in gene ADA2 reported as likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001282225.2(ADA2):c.1045G>A (p.Val349Ile)	rs74317375	0.00227
NM_001282225.2(ADA2):c.927G>A (p.Met309Ile)	rs146597836	0.00156
NM_001282225.2(ADA2):c.1386T>C (p.Ile462=)	rs373797039	0.00051
NM_001282225.2(ADA2):c.1467G>C (p.Glu489Asp)	rs61738625	0.00041
NM_001282225.2(ADA2):c.147G>A (p.Arg49=)	rs146125672	0.00013
NM_001282225.2(ADA2):c.702G>A (p.Glu234=)	rs528271447	0.00005
NM_001282225.2(ADA2):c.1146C>T (p.Ile382=)	rs776302859	0.00001
NM_001282225.2(ADA2):c.1071C>T (p.Ala357=)	rs144447953
NM_001282225.2(ADA2):c.138G>T (p.Leu46=)	rs7289141
NM_001282225.2(ADA2):c.1497G>A (p.Lys499=)	rs2123598853
NM_001282225.2(ADA2):c.87C>T (p.Ser29=)

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