List of variants in gene MAP2K2 reported as benign by Baylor Genetics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.660C>A (p.Ile220=)	rs10250	0.42547
NM_030662.4(MAP2K2):c.453C>T (p.Asp151=)	rs17851657	0.13902
NM_030662.4(MAP2K2):c.405G>C (p.Gly135=)	rs10424722	0.04706

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