List of variants in gene MAP2K2 reported as benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.405G>C (p.Gly135=)	rs10424722	0.04706
NM_030662.4(MAP2K2):c.-243C>T	rs181533374	0.04405
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.498C>T (p.Pro166=)	rs139404261	0.00076
NM_030662.4(MAP2K2):c.1140C>T (p.Ala380=)	rs146618055	0.00034
NM_030662.4(MAP2K2):c.893C>T (p.Pro298Leu)	rs200371894	0.00034
NM_030662.4(MAP2K2):c.525C>T (p.Ile175=)	rs150833333	0.00029
NM_030662.4(MAP2K2):c.420C>T (p.Asp140=)	rs369925884	0.00016
NM_030662.4(MAP2K2):c.1020C>T (p.Pro340=)	rs192389729	0.00009
NM_030662.4(MAP2K2):c.1198G>A (p.Val400Met)	rs533247725	0.00005
NM_030662.4(MAP2K2):c.141C>T (p.Asp47=)	rs201526172	0.00003

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