"Genome-Nilou Lab"[submitter] AND "SLC30A9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1242979	NM_006345.4(SLC30A9):c.9C>G (p.Pro3=)	SLC30A9	Single nucleotide variant (synonymous variant)	Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome +1 more	GBenign
Select item 1333130	NM_006345.4(SLC30A9):c.148A>G (p.Met50Val)	SLC30A9 (M50V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1333131	NM_006345.4(SLC30A9):c.274+38C>G	SLC30A9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1333132	NM_006345.4(SLC30A9):c.289A>G (p.Thr97Ala)	SLC30A9 (T97A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1333133	NM_006345.4(SLC30A9):c.366C>A (p.Gly122=)	SLC30A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1333134	NM_006345.4(SLC30A9):c.527+35A>G	SLC30A9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar