List of variants in gene MAP2K2 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.919+12A>G	rs350911	0.74641
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.192C>T (p.Val64=)	rs8157	0.06496
NM_030662.4(MAP2K2):c.450+15G>T	rs10424545	0.04749
NM_030662.4(MAP2K2):c.405G>C (p.Gly135=)	rs10424722	0.04706
NM_030662.4(MAP2K2):c.846C>T (p.Pro282=)	rs11539506	0.00282
NM_030662.4(MAP2K2):c.580+6G>A	rs201435249	0.00183
NM_030662.4(MAP2K2):c.303+11C>T	rs200405512	0.00179
NM_030662.4(MAP2K2):c.303+8C>G	rs199612401	0.00054
NM_030662.4(MAP2K2):c.893C>T (p.Pro298Leu)	rs200371894	0.00034
NM_030662.4(MAP2K2):c.420C>T (p.Asp140=)	rs369925884	0.00016
NM_030662.4(MAP2K2):c.981C>T (p.Asn327=)	rs143275018	0.00011
NM_030662.4(MAP2K2):c.1020C>T (p.Pro340=)	rs192389729	0.00009
NM_030662.4(MAP2K2):c.705+11G>C	rs202086678

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