List of variants in gene combination LOC130056094, NPC2 reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006432.4(NPC2):c.-89G>A	rs574247323	0.00001
NM_006432.4(NPC2):c.-68G>T	rs578161135

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