List of variants in gene IL12RB1 reported as likely benign for Immunodeficiency 27A

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: 4

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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	0.11978
NM_005535.3(IL12RB1):c.783+10C>T	rs79972275	0.00554
NM_005535.3(IL12RB1):c.1719C>T (p.Ala573=)	rs17885102	0.00316

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