Related gene-specific medical variations for Gene (Select 101928278) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3108615	NM_000599.4(IGFBP5):c.50C>G (p.Pro17Arg)	IGFBP-AS1, IGFBP5 (P17R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2621848	NM_000599.4(IGFBP5):c.286G>A (p.Gly96Ser)	IGFBP-AS1, IGFBP5 (G96S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2598971	NM_000599.4(IGFBP5):c.118C>G (p.Pro40Ala)	IGFBP-AS1, IGFBP5 (P40A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2551411	NM_000599.4(IGFBP5):c.115C>T (p.Pro39Ser)	IGFBP-AS1, IGFBP5 (P39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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