Related gene-specific medical variations for Gene (Select 64924) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690009	NM_022902.5(SLC30A5):c.719T>G (p.Leu240Ter)	SLC30A5 (L240*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2685158	GRCh37/hg19 5q13.1-13.2(chr5:67725323-68414933)x1	SLC30A5	Copy number loss	not provided	GUncertain significance
Select item 2324282	NM_022902.5(SLC30A5):c.31G>A (p.Ala11Thr)	LOC129994018, SLC30A5 (A11T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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