List of variants in gene PIGO reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_032634.4(PIGO):c.2040G>C (p.Leu680=)	rs41274877	0.00511
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.3163T>C (p.Phe1055Leu)	rs147316771	0.00093
NM_032634.4(PIGO):c.626A>G (p.Asn209Ser)	rs138028827	0.00084
NM_032634.4(PIGO):c.1662G>A (p.Leu554=)	rs369433160	0.00006
NM_032634.4(PIGO):c.789G>A (p.Val263=)	rs750328169	0.00004
NM_032634.4(PIGO):c.1918C>T (p.Arg640Cys)	rs552540556	0.00002
NM_032634.4(PIGO):c.*8TG[1]	rs540040672
NM_032634.4(PIGO):c.246C>T (p.Phe82=)	rs748671184
NM_032634.4(PIGO):c.2979G>A (p.Leu993=)	rs1554672011

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