Variants in gene IL12RB1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005535.3(IL12RB1):c.641A>G (p.Gln214Arg)	rs11575934	0.25155
NM_005535.3(IL12RB1):c.467G>A (p.Arg156His)	rs11575926	0.12190
NM_005535.3(IL12RB1):c.783+10C>T	rs79972275	0.00537
NM_005535.3(IL12RB1):c.1573G>A (p.Ala525Thr)	rs11575935	0.00494
NM_005535.3(IL12RB1):c.180C>T (p.Tyr60=)	rs146102898	0.00243
NM_005535.3(IL12RB1):c.1098G>A (p.Thr366=)	rs61734350	0.00234

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