SLC39A9[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3319783	NM_018375.5(SLC39A9):c.107A>G (p.Lys36Arg)	SLC39A9 (K36R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164735	NM_018375.5(SLC39A9):c.296A>G (p.His99Arg)	SLC39A9 (H99R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3319782	NM_018375.5(SLC39A9):c.386A>G (p.His129Arg)	SLC39A9 (H11R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 781132	NM_018375.5(SLC39A9):c.735G>A (p.Val245=)	SLC39A9	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3164736	NM_018375.5(SLC39A9):c.826G>A (p.Asp276Asn)	SLC39A9 (D276N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3319784	NM_018375.5(SLC39A9):c.854G>T (p.Arg285Leu)	SLC39A9 (R285L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384628	NM_018375.5(SLC39A9):c.854G>A (p.Arg285His)	SLC39A9 (R167H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164737	NM_018375.5(SLC39A9):c.891C>G (p.Ile297Met)	SLC39A9 (I297M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar