"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126806104" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 893814	NM_001206744.2(TPO):c.2652C>G (p.Ile884Met)	LOC126806104, TPO (I840M +3 more)	Single nucleotide variant (missense variant)	Deficiency of iodide peroxidase	GUncertain significance
Select item 893815	NM_001206744.2(TPO):c.2691A>T (p.Gly897=)	LOC126806104, TPO	Single nucleotide variant (synonymous variant)	Deficiency of iodide peroxidase	GUncertain significance
Select item 331638	NM_001206744.2(TPO):c.2702C>G (p.Ala901Gly)	LOC126806104, TPO (A901G +3 more)	Single nucleotide variant (missense variant)	Deficiency of iodide peroxidase	GUncertain significance
Select item 331639	NM_001206744.2(TPO):c.2703C>T (p.Ala901=)	LOC126806104, TPO	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 893816	NM_001206744.2(TPO):c.2704G>T (p.Val902Leu)	TPO, LOC126806104 (V729L +3 more)	Single nucleotide variant (missense variant)	Deficiency of iodide peroxidase	GUncertain significance
Select item 331640	NM_001206744.2(TPO):c.2717C>T (p.Pro906Leu)	LOC126806104, TPO (P906L +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar