ClinVar Miner

List of variants in gene PIGN reported as pathogenic by Undiagnosed Diseases Network, NIH

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_176787.5(PIGN):c.932T>G (p.Leu311Trp)	rs746882521	0.00005
NM_176787.5(PIGN):c.1251+1G>A	rs1462805697	0.00003

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