List of variants in gene PIGN reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_176787.5(PIGN):c.685C>G (p.His229Asp)	rs9320001	0.79552
NM_176787.5(PIGN):c.741C>T (p.His247=)	rs9320000	0.56637
NM_176787.5(PIGN):c.939T>C (p.Asn313=)	rs34227891	0.24195
NM_176787.5(PIGN):c.806-7T>A	rs61751989	0.21786
NM_176787.5(PIGN):c.1962G>A (p.Leu654=)	rs12326381	0.17264
NM_176787.5(PIGN):c.1245T>C (p.Asp415=)	rs13381627	0.17246
NM_176787.5(PIGN):c.2010T>C (p.Thr670=)	rs17714063	0.17242
NM_176787.5(PIGN):c.1752G>A (p.Leu584=)	rs9319997	0.17086
NM_176787.5(PIGN):c.1377T>C (p.Ser459=)	rs17714875	0.16805
NM_176787.5(PIGN):c.484A>G (p.Lys162Glu)	rs17069506	0.04997

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