List of variants in gene MAP2K2 reported as uncertain significance for immune system disorder

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.1162C>T (p.Arg388Trp)	rs144383241	0.00222
NM_030662.4(MAP2K2):c.844C>T (p.Pro282Ser)	rs142307980	0.00070
NM_030662.4(MAP2K2):c.853G>A (p.Asp285Asn)	rs150369301	0.00008
NM_030662.4(MAP2K2):c.938G>A (p.Arg313Gln)	rs151133017	0.00004
NM_030662.4(MAP2K2):c.326C>T (p.Pro109Leu)	rs544242665	0.00002
NM_030662.4(MAP2K2):c.1109A>G (p.Lys370Arg)	rs1599278009
NM_030662.4(MAP2K2):c.183A>T (p.Lys61Asn)	rs886041310
NM_030662.4(MAP2K2):c.523A>G (p.Ile175Val)	rs373325880

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