List of variants in gene combination IL2RG, LOC126863274 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000206.3(IL2RG):c.78A>T (p.Thr26=)	rs147424359	0.00023
NM_000206.3(IL2RG):c.86C>T (p.Thr29Met)	rs375921454	0.00009
NM_000206.3(IL2RG):c.92A>G (p.Asn31Ser)	rs749977756	0.00007
NM_000206.3(IL2RG):c.69G>A (p.Leu23=)	rs748252421	0.00003
NM_000206.3(IL2RG):c.75G>A (p.Thr25=)	rs754951792	0.00002
NM_000206.3(IL2RG):c.87G>A (p.Thr29=)	rs779772745	0.00002
NM_000206.3(IL2RG):c.92A>T (p.Asn31Ile)

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