List of variants in gene PIGO reported as benign by Invitae

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_032634.4(PIGO):c.1119+7A>G	rs568300	0.52243
NM_032634.4(PIGO):c.2004G>A (p.Leu668=)	rs10814196	0.19210
NM_032634.4(PIGO):c.3114C>T (p.Leu1038=)	rs2298314	0.02715
NM_032634.4(PIGO):c.1404A>C (p.Ala468=)	rs35287398	0.01214
NM_032634.4(PIGO):c.423C>T (p.Gly141=)	rs116248521	0.01090
NM_032634.4(PIGO):c.1120-15C>A	rs77344591	0.00631
NM_032634.4(PIGO):c.2432G>A (p.Arg811Gln)	rs75579358	0.00578
NM_032634.4(PIGO):c.1473G>C (p.Leu491=)	rs76932500	0.00557
NM_032634.4(PIGO):c.2040G>C (p.Leu680=)	rs41274877	0.00511
NM_032634.4(PIGO):c.2268G>A (p.Ala756=)	rs149171782	0.00310
NM_032634.4(PIGO):c.461C>A (p.Ala154Asp)	rs142562923	0.00277
NM_032634.4(PIGO):c.2166G>C (p.Ala722=)	rs147101825	0.00143
NM_032634.4(PIGO):c.2124G>A (p.Leu708=)	rs201657672	0.00095
NM_032634.4(PIGO):c.2487G>T (p.Gly829=)	rs763623508	0.00019
NM_032634.4(PIGO):c.2198G>A (p.Arg733Gln)	rs373305585	0.00004
NM_032634.4(PIGO):c.2520C>T (p.Leu840=)	rs537796918
NM_032634.4(PIGO):c.2563A>G (p.Ile855Val)
NM_032634.4(PIGO):c.2854+8del	rs756312077
NM_032634.4(PIGO):c.512-17C>T	rs2240116
NM_032634.4(PIGO):c.714C>T (p.Gly238=)	rs148186264

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