Related gene-specific medical variations for Gene (Select 387836) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2621932	NM_001190765.1(KLRF2):c.115G>C (p.Gly39Arg)	CLEC2A, KLRF2 (G39R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458052	NM_001190765.1(KLRF2):c.314A>T (p.Asp105Val)	CLEC2A, KLRF2 (D105V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457173	NM_001190765.1(KLRF2):c.26C>T (p.Thr9Met)	CLEC2A, KLRF2 (T9M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2386183	NM_001190765.1(KLRF2):c.599C>T (p.Thr200Met)	CLEC2A, KLRF2 (T200M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2384950	NM_001190765.1(KLRF2):c.268T>C (p.Tyr90His)	CLEC2A, KLRF2 (Y90H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2354440	NM_001190765.1(KLRF2):c.526A>T (p.Thr176Ser)	KLRF2, CLEC2A (T176S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335500	NM_001190765.1(KLRF2):c.310C>T (p.Arg104Cys)	CLEC2A, KLRF2 (R104C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314222	NM_001190765.1(KLRF2):c.402T>G (p.Phe134Leu)	CLEC2A, KLRF2 (F134L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291336	NM_001190765.1(KLRF2):c.119G>A (p.Cys40Tyr)	KLRF2, CLEC2A (C40Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2269914	NM_001190765.1(KLRF2):c.348T>G (p.Ile116Met)	KLRF2, CLEC2A (I116M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261335	NM_001190765.1(KLRF2):c.191A>C (p.Gln64Pro)	KLRF2, CLEC2A (Q64P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252803	NM_001190765.1(KLRF2):c.259G>A (p.Gly87Arg)	KLRF2, CLEC2A (G87R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251728	NM_001190765.1(KLRF2):c.236C>T (p.Pro79Leu)	CLEC2A, KLRF2 (P79L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251727	NM_001190765.1(KLRF2):c.222C>G (p.His74Gln)	CLEC2A, KLRF2 (H74Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance