Related gene-specific medical variations for Gene (Select 8550) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2339558	NM_003668.4(MAPKAPK5):c.31A>G (p.Ile11Val)	MAPKAPK5-AS1, MAPKAPK5 (I11V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2294416	NM_003668.4(MAPKAPK5):c.17A>G (p.Asp6Gly)	MAPKAPK5, MAPKAPK5-AS1 (S6P +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance