ClinVar Miner

List of variants in gene INPP5E reported as uncertain significance 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
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_019892.6(INPP5E):c.1408G>A (p.Asp470Asn)	rs1835717140	0.00001
NM_019892.6(INPP5E):c.856G>A (p.Gly286Arg)	rs757936530	0.00001

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