"Illumina Laboratory Services, Illumina"[submitter] AND "LOC129934140" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 337130	NM_013247.5(HTRA2):c.507-10T>A	HTRA2, LOC129934140	Single nucleotide variant (intron variant)	Parkinson disease 13, autosomal dominant, susceptibility to	GUncertain significance
Select item 337131	NM_013247.5(HTRA2):c.507-9C>A	LOC129934140, HTRA2	Single nucleotide variant (intron variant)	Parkinson disease 13, autosomal dominant, susceptibility to	GUncertain significance