ClinVar Miner

List of variants in gene PNPO reported as not provided by GenomeConnect - Invitae Patient Insights Network

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_018129.4(PNPO):c.422G>A (p.Arg141His)	rs759335202	0.00001
NM_018129.4(PNPO):c.759C>G (p.Asp253Glu)	rs757023013

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