Related gene-specific medical variations for Gene (Select 283869) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2556697	NM_001099456.3(NPW):c.488G>T (p.Gly163Val)	LOC125146377, NPW (G163V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533819	NM_001099456.3(NPW):c.473C>A (p.Pro158His)	NPW, LOC125146377 (P158H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224245	NM_001099456.3(NPW):c.433C>G (p.Arg145Gly)	LOC125146377, NPW (R145G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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