Related gene-specific medical variations for Gene (Select 3384) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3285175	NM_001099789.2(ICAM2):c.346A>G (p.Ile116Val)	ICAM2, PRR29 (I116V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285174	NM_001099789.2(ICAM2):c.635T>C (p.Met212Thr)	ICAM2, PRR29 (M212T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285173	NM_001099789.2(ICAM2):c.707C>T (p.Ser236Phe)	ICAM2, PRR29 (S236F)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3285172	NM_001099789.2(ICAM2):c.539A>G (p.Asp180Gly)	ICAM2, PRR29 (D180G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285170	NM_001099789.2(ICAM2):c.542G>A (p.Arg181Lys)	ICAM2, PRR29 (R181K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107895	NM_001099789.2(ICAM2):c.784G>A (p.Val262Met)	ICAM2, PRR29 (V262M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107893	NM_001099789.2(ICAM2):c.598G>A (p.Gly200Ser)	ICAM2, PRR29 (G200S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620709	NM_001099789.2(ICAM2):c.692T>C (p.Val231Ala)	ICAM2, PRR29 (V231A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592622	NM_001099789.2(ICAM2):c.758G>A (p.Arg253His)	ICAM2, PRR29 (R253H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2514972	NM_001099789.2(ICAM2):c.484G>A (p.Gly162Arg)	ICAM2, PRR29 (G162R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454334	NM_001099789.2(ICAM2):c.714C>G (p.Phe238Leu)	PRR29, ICAM2 (F238L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341127	NM_001099789.2(ICAM2):c.395T>C (p.Ile132Thr)	ICAM2, PRR29 (I132T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296208	NM_001099789.2(ICAM2):c.421C>G (p.Pro141Ala)	ICAM2, PRR29 (P141A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281394	NM_001099789.2(ICAM2):c.431G>A (p.Ser144Asn)	ICAM2, PRR29 (S144N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214426	NM_001099789.2(ICAM2):c.788G>A (p.Arg263Gln)	ICAM2, PRR29 (R263Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign