Related gene-specific medical variations for Gene (Select 6279) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606720	NM_176823.4(S100A7A):c.274G>A (p.Gly92Arg)	S100A7A, S100A8 (G92R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2597946	NM_176823.4(S100A7A):c.281C>T (p.Ala94Val)	S100A7A, S100A8 (A94V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2554524	NM_176823.4(S100A7A):c.85A>G (p.Lys29Glu)	S100A7A, S100A8 (K29E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2511126	NM_176823.4(S100A7A):c.175T>C (p.Phe59Leu)	S100A7A, S100A8 (F59L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2398754	NM_176823.4(S100A7A):c.155T>C (p.Ile52Thr)	S100A7A, S100A8 (I52T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2398664	NM_176823.4(S100A7A):c.157C>A (p.His53Asn)	S100A7A, S100A8 (H53N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2362756	NM_002964.5(S100A8):c.217A>T (p.Ile73Phe)	LOC129388608, S100A8 (I81F +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330182	NM_176823.4(S100A7A):c.270C>G (p.Ser90Arg)	S100A7A, S100A8 (S90R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2299153	NM_176823.4(S100A7A):c.87G>T (p.Lys29Asn)	S100A7A, S100A8 (K29N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2274755	NM_176823.4(S100A7A):c.290C>A (p.Ser97Tyr)	S100A7A, S100A8 (S97Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2260418	NM_002964.5(S100A8):c.151G>A (p.Ala51Thr)	LOC129388608, S100A8 (A51T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance