List of variants in gene MAP2K2 reported as likely pathogenic for not provided

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.787G>A (p.Gly263Arg)	rs730880522	0.00002
NM_030662.4(MAP2K2):c.181A>G (p.Lys61Glu)	rs730880517
NM_030662.4(MAP2K2):c.183A>C (p.Lys61Asn)	rs886041310
NM_030662.4(MAP2K2):c.190G>T (p.Val64Phe)	rs730880518
NM_030662.4(MAP2K2):c.395G>A (p.Gly132Asp)	rs387906800
NM_030662.4(MAP2K2):c.619G>A (p.Glu207Lys)	rs727504382

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