"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC39A8"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051072	NM_001135147.1(SLC39A8):c.1267-4G>C	SLC39A8	Single nucleotide variant (intron variant)	SLC39A8-related disorder	GLikely benign
Select item 3032541	NM_001135146.2(SLC39A8):c.1049-17TCT[6]	LOC126807125, SLC39A8	Microsatellite (intron variant)	SLC39A8-related disorder	GLikely benign
Select item 3046833	NM_001135146.2(SLC39A8):c.951C>T (p.Ile317=)	LOC126807125, SLC39A8	Single nucleotide variant (synonymous variant)	SLC39A8-related disorder	GLikely benign
Select item 732461	NM_001135146.2(SLC39A8):c.745C>G (p.Pro249Ala)	SLC39A8 (P249A +1 more)	Single nucleotide variant (missense variant)	SLC39A8-related disorder +1 more	GBenign/Likely benign
Select item 2223788	NM_001135146.2(SLC39A8):c.676-4A>G	SLC39A8	Single nucleotide variant (intron variant)	SLC39A8-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 743544	NM_001135146.2(SLC39A8):c.477A>G (p.Pro159=)	SLC39A8	Single nucleotide variant (synonymous variant)	SLC39A8-related disorder +1 more	GLikely benign
Select item 719671	NM_001135146.2(SLC39A8):c.81A>C (p.Leu27=)	LOC129992876, SLC39A8	Single nucleotide variant (synonymous variant)	SLC39A8-related disorder +1 more	GBenign/Likely benign

ClinVar