List of variants in gene PIGN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_176787.5(PIGN):c.528G>A (p.Thr176=)	rs144304758	0.00291
NM_176787.5(PIGN):c.1617T>C (p.Tyr539=)	rs147306123	0.00282
NM_176787.5(PIGN):c.2751G>T (p.Thr917=)	rs200481058	0.00183
NM_176787.5(PIGN):c.2022A>G (p.Leu674=)	rs3764491	0.00049
NM_176787.5(PIGN):c.364G>C (p.Glu122Gln)	rs200756305	0.00043
NM_176787.5(PIGN):c.1749G>A (p.Arg583=)	rs200401462	0.00025
NM_176787.5(PIGN):c.1707C>T (p.Thr569=)	rs375845698	0.00019
NM_176787.5(PIGN):c.459C>T (p.His153=)	rs376615257	0.00019
NM_176787.5(PIGN):c.253A>G (p.Ile85Val)	rs202066215	0.00018
NM_176787.5(PIGN):c.2448T>C (p.Tyr816=)	rs368921294	0.00010
NM_176787.5(PIGN):c.882A>G (p.Gln294=)	rs1376888820	0.00001
NM_176787.5(PIGN):c.1605A>C (p.Ser535=)	rs755115652
NM_176787.5(PIGN):c.1869A>G (p.Ala623=)	rs763671604
NM_176787.5(PIGN):c.2736C>G (p.Ala912=)

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