List of variants in gene ADA2 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001282225.2(ADA2):c.506G>A (p.Arg169Gln)	rs77563738	0.00041
NM_001282225.2(ADA2):c.139G>A (p.Gly47Arg)	rs202134424	0.00010
NM_001282225.2(ADA2):c.1358A>G (p.Tyr453Cys)	rs376785840	0.00007
NM_001282225.2(ADA2):c.1147G>A (p.Gly383Ser)	rs770689762	0.00004
NM_001282225.2(ADA2):c.752C>T (p.Pro251Leu)	rs148936893	0.00004
NM_001282225.2(ADA2):c.336C>G (p.His112Gln)	rs587777241	0.00002
NM_001282225.2(ADA2):c.1078A>G (p.Thr360Ala)	rs775440641	0.00001
NM_001282225.2(ADA2):c.1225C>T (p.Pro409Ser)	rs777618863
NM_001282225.2(ADA2):c.140G>C (p.Gly47Ala)	rs200930463
NM_001282225.2(ADA2):c.140G>T (p.Gly47Val)	rs200930463
NM_001282225.2(ADA2):c.326C>A (p.Ala109Asp)	rs587777240
NM_001282225.2(ADA2):c.631TTC[1] (p.Phe212del)	rs2123699776
NM_001282225.2(ADA2):c.791G>C (p.Trp264Ser)	rs587777242

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