"Illumina Laboratory Services, Illumina"[submitter] AND "LOC130055387" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 312940	NM_001354768.3(NRL):c.*56G>A	LOC130055387, NRL	Single nucleotide variant (3 prime UTR variant)	Retinitis pigmentosa	GUncertain significance
Select item 167386	NM_001354768.3(NRL):c.711C>G (p.Leu237=)	LOC130055387, NRL	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 882486	NM_001354768.3(NRL):c.645C>T (p.Tyr215=)	LOC130055387, NRL	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity

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ClinVar