List of variants in gene combination IL2RG, LOC126863274 reported as likely 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: 17

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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.51C>T (p.Pro17=)	rs773483114	0.00009
NM_000206.3(IL2RG):c.86C>T (p.Thr29Met)	rs375921454	0.00009
NM_000206.3(IL2RG):c.74C>T (p.Thr25Met)	rs751455361	0.00005
NM_000206.3(IL2RG):c.116-5T>G	rs754256514	0.00002
NM_000206.3(IL2RG):c.75G>A (p.Thr25=)	rs754951792	0.00002
NM_000206.3(IL2RG):c.37T>C (p.Phe13Leu)	rs1015272346	0.00001
NM_000206.3(IL2RG):c.115+10C>T
NM_000206.3(IL2RG):c.116-14T>A
NM_000206.3(IL2RG):c.116-8C>T
NM_000206.3(IL2RG):c.124C>T (p.Leu42=)
NM_000206.3(IL2RG):c.15A>G (p.Ser5=)
NM_000206.3(IL2RG):c.15A>T (p.Ser5=)	rs2147751939
NM_000206.3(IL2RG):c.30C>T (p.Ser10=)
NM_000206.3(IL2RG):c.60A>C (p.Gly20=)	rs772095231
NM_000206.3(IL2RG):c.60A>G (p.Gly20=)
NM_000206.3(IL2RG):c.72C>T (p.Asn24=)

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