List of variants in gene combination IL2RA, LOC130003232 reported as uncertain significance for immune system disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000417.3(IL2RA):c.45G>A (p.Met15Ile)	rs74162092	0.00001
NM_000417.3(IL2RA):c.40A>G (p.Ile14Val)	rs781222262

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