Variants in gene IL7R with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_002185.5(IL7R):c.197T>C (p.Ile66Thr)	rs1494558	0.68368
NM_002185.5(IL7R):c.561G>A (p.Lys187=)	rs11567764	0.03877
NM_002185.5(IL7R):c.*42A>G	rs145513117	0.00647
NM_002185.5(IL7R):c.1231A>G (p.Thr411Ala)	rs115316501	0.00398
NM_002185.5(IL7R):c.132C>T (p.Ser44=)	rs11567704	0.00357
NM_002185.5(IL7R):c.1020T>G (p.Leu340=)	rs138731184	0.00096
NM_002185.5(IL7R):c.1043A>C (p.Asn348Thr)	rs41270321

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