List of variants in gene IL7R reported as likely benign by Illumina Laboratory Services, Illumina

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002185.5(IL7R):c.561G>A (p.Lys187=)	rs11567764	0.03877
NM_002185.5(IL7R):c.132C>T (p.Ser44=)	rs11567704	0.00357
NM_002185.5(IL7R):c.*3089C>T	rs187963551	0.00235
NM_002185.5(IL7R):c.778G>A (p.Ala260Thr)	rs147153824	0.00144
NM_002185.5(IL7R):c.*2429T>C	rs548166315	0.00138
NM_002185.5(IL7R):c.1020T>G (p.Leu340=)	rs138731184	0.00096
NM_002185.5(IL7R):c.*651C>G	rs77118170	0.00016
NM_002185.5(IL7R):c.*1902del	rs33994244
NM_002185.5(IL7R):c.*334AAAG[4]	rs397691511

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