List of variants in gene IDH2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002168.4(IDH2):c.996C>T (p.Ser332=)	rs61737003	0.07655
NM_002168.4(IDH2):c.1050C>T (p.Thr350=)	rs11540478	0.05301
NM_002168.4(IDH2):c.993G>A (p.Thr331=)	rs61737002	0.01104
NM_002168.4(IDH2):c.429G>C (p.Leu143=)	rs144712130	0.00824
NM_002168.4(IDH2):c.1304C>T (p.Thr435Met)	rs118053940	0.00372
NM_002168.4(IDH2):c.939A>G (p.Gly313=)	rs16943901	0.00280
NM_002168.4(IDH2):c.782G>A (p.Arg261His)	rs118101777	0.00163
NM_002168.4(IDH2):c.673G>A (p.Asp225Asn)	rs142816010	0.00035
NM_002168.4(IDH2):c.890T>C (p.Val297Ala)	rs538460237	0.00017
NM_002168.4(IDH2):c.360G>A (p.Glu120=)	rs536071174	0.00011
NM_002168.4(IDH2):c.695C>T (p.Ala232Val)	rs1227626398

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