ClinVar Miner

List of variants in gene combination NPC1, RMC1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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: 4

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HGVS	dbSNP
NM_000271.5(NPC1):c.*485dup	rs757215027
NM_000271.5(NPC1):c.*494G>T
NM_000271.5(NPC1):c.*500A>G	rs886053662
NM_000271.5(NPC1):c.*718C>T

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