List of variants in gene combination ADA, LOC107303343 reported as benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000022.4(ADA):c.36G>A (p.Val12=)	rs394105	0.98470
NM_000022.4(ADA):c.95+165A>G	rs967807	0.90213
NM_000022.3(ADA):c.-101G>A	rs36216718	0.04373
NM_000022.2(ADA):c.22G>A (p.Asp8Asn)	rs73598374	0.04175
NM_000022.4(ADA):c.36= (p.Val12=)	rs394105	0.01530
NM_000022.4(ADA):c.95+9A>G	rs765216	0.00319
NM_000022.4(ADA):c.162G>A (p.Lys54=)	rs45557242	0.00282
NM_000022.4(ADA):c.192G>A (p.Lys64=)	rs144168646	0.00009
NM_000022.4(ADA):c.33+17dup	rs1246752878
NM_000022.4(ADA):c.34-7del	rs1297398786

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