List of variants in gene IL2RA 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000417.3(IL2RA):c.368-18A>G	rs942200	0.89057
NM_000417.3(IL2RA):c.*1267G>A	rs1570538	0.41693
NM_000417.3(IL2RA):c.*1461T>C	rs12244380	0.40803
NM_000417.3(IL2RA):c.367+12A>T	rs12358961	0.30992
NM_000417.3(IL2RA):c.367+7G>C	rs11256369	0.20897
NM_000417.3(IL2RA):c.*1702C>T	rs12722606	0.15795
NM_000417.2(IL2RA):c.*2191T>G	rs12722609	0.11171
NM_000417.3(IL2RA):c.*1672A>T	rs12722605	0.10759
NM_000417.3(IL2RA):c.*969G>A	rs12722602	0.10647
NM_000417.3(IL2RA):c.656-17T>G	rs28360490	0.08627
NM_000417.3(IL2RA):c.84G>A (p.Pro28=)	rs2228150	0.08221
NM_000417.3(IL2RA):c.516C>T (p.His172=)	rs2228149	0.05507
NM_000417.3(IL2RA):c.*1994G>T	rs12722608	0.05407
NM_000417.3(IL2RA):c.*677G>A	rs12719919	0.04736
NM_000417.3(IL2RA):c.*1880C>G	rs12722607	0.04629
NM_000417.3(IL2RA):c.*1549C>T	rs12722604	0.03738
NM_000417.3(IL2RA):c.753C>T (p.Ile251=)	rs12722698	0.01814
NM_000417.3(IL2RA):c.*70G>A	rs12722600	0.01782
NM_000417.3(IL2RA):c.*1024G>A	rs12722718	0.00760
NM_000417.3(IL2RA):c.*55T>C	rs12722713	0.00759
NM_000417.3(IL2RA):c.65-20A>G	rs12722687	0.00558
NM_000417.3(IL2RA):c.272C>T (p.Thr91Met)	rs72650666	0.00183
NM_000417.3(IL2RA):c.*2108T>G	rs74895246	0.00171
NM_000417.3(IL2RA):c.*1008G>A	rs34164172	0.00170
NM_000417.3(IL2RA):c.711A>G (p.Thr237=)	rs11256354	0.00053
NM_000417.3(IL2RA):c.368-16T>C	rs191340172	0.00018
NM_000417.3(IL2RA):c.457G>A (p.Val153Ile)	rs201188114	0.00009
NM_000417.3(IL2RA):c.64+15308T>A	rs12722508

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