ClinVar Miner

List of variants in gene NPRL2 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006545.5(NPRL2):c.995G>A (p.Arg332Gln)	rs587660975	0.00003
NM_006545.5(NPRL2):c.1080G>A (p.Met360Ile)	rs1393501650
NM_006545.5(NPRL2):c.932G>A (p.Arg311Gln)	rs769961301

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