List of variants in gene MAP2K2 reported as benign for ectodermal dysplasia syndrome

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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_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.405G>C (p.Gly135=)	rs10424722	0.04706
NM_030662.4(MAP2K2):c.303+18G>A	rs116988721	0.00894
NM_030662.4(MAP2K2):c.846C>T (p.Pro282=)	rs11539506	0.00282
NM_030662.4(MAP2K2):c.1093-6T>C	rs369681843	0.00065
NM_030662.4(MAP2K2):c.581-8G>A	rs369262004	0.00012
NM_030662.4(MAP2K2):c.690G>A (p.Thr230=)	rs201287884	0.00005
NM_030662.4(MAP2K2):c.705+11G>C	rs202086678

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