List of variants in gene IL12RB1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005535.3(IL12RB1):c.1094T>C (p.Met365Thr)	rs375947	0.29555
NM_005535.3(IL12RB1):c.1132G>C (p.Gly378Arg)	rs401502	0.28523
NM_005535.3(IL12RB1):c.641A>G (p.Gln214Arg)	rs11575934	0.25155
NM_005535.3(IL12RB1):c.-2C>T	rs436857	0.17226
NM_005535.3(IL12RB1):c.467G>A (p.Arg156His)	rs11575926	0.12190
NM_005535.3(IL12RB1):c.387G>C (p.Val129=)	rs11086087	0.09792
NM_005535.3(IL12RB1):c.684C>T (p.Pro228=)	rs17852635

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