Related gene-specific medical variations for Gene (Select 105372397) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2601980	NM_001042600.3(MAP4K1):c.1489C>T (p.Arg497Trp)	MAP4K1, MAP4K1-AS1 (R497W)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534128	NM_001042600.3(MAP4K1):c.1536G>T (p.Gln512His)	MAP4K1, MAP4K1-AS1 (Q512H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2512846	NM_001042600.3(MAP4K1):c.1598C>T (p.Thr533Met)	MAP4K1, MAP4K1-AS1 (T533M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463727	NM_001042600.3(MAP4K1):c.2003C>G (p.Ser668Cys)	MAP4K1, MAP4K1-AS1 (S668C)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2410558	NM_001042600.3(MAP4K1):c.1885A>G (p.Thr629Ala)	MAP4K1, MAP4K1-AS1 (T629A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2397055	NM_001042600.3(MAP4K1):c.1826C>T (p.Ala609Val)	MAP4K1, MAP4K1-AS1 (A609V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2278849	NM_001042600.3(MAP4K1):c.1982C>G (p.Ala661Gly)	MAP4K1-AS1, MAP4K1 (A661G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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