Related gene-specific medical variations for Gene (Select 29986) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3319754	NM_014579.4(SLC39A2):c.296A>T (p.His99Leu)	LOC126861883, SLC39A2 (H99L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3319753	NM_014579.4(SLC39A2):c.55A>C (p.Thr19Pro)	LOC126861883, SLC39A2 (T19P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319752	NM_014579.4(SLC39A2):c.94T>C (p.Phe32Leu)	LOC126861883, SLC39A2 (F32L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164667	NM_014579.4(SLC39A2):c.201A>C (p.Glu67Asp)	LOC126861883, SLC39A2 (E67D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164666	NM_014579.4(SLC39A2):c.190A>G (p.Met64Val)	LOC126861883, SLC39A2 (M64V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336888	NM_014579.4(SLC39A2):c.252A>T (p.Arg84Ser)	LOC126861883, SLC39A2 (I83F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296316	NM_014579.4(SLC39A2):c.64T>C (p.Cys22Arg)	LOC126861883, SLC39A2 (C22R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1243818	NM_014579.4(SLC39A2):c.128T>G (p.Leu43Arg)	LOC126861883, SLC39A2 (L43R)	Single nucleotide variant (missense variant)	not provided	GBenign

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