"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SLC39A11"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2648171	NM_139177.4(SLC39A11):c.348C>T (p.Phe116=)	LOC126862633, SLC39A11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648172	NM_139177.4(SLC39A11):c.60G>A (p.Gly20=)	SLC39A11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 624519	GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3	LLGL2, MAP2K6 +119 more	Copy number gain	not provided	GLikely pathogenic

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