"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126861662" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 307487	NM_002150.3(HPD):c.294C>T (p.Phe98=)	HPD, LOC126861662	Single nucleotide variant (synonymous variant)	Hawkinsinuria +1 more	GConflicting classifications of pathogenicity
Select item 307488	NM_002150.3(HPD):c.211C>G (p.Leu71Val)	HPD, LOC126861662 (L32V +1 more)	Single nucleotide variant (missense variant)	Hawkinsinuria +1 more	GUncertain significance