List of variants in gene PIK3C2G reported as uncertain significance by Martin Pollak Laboratory, Beth Israel Deaconess Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001288772.2(PIK3C2G):c.1077A>T (p.Lys359Asn)	rs373231729	0.00013
NM_001288772.2(PIK3C2G):c.2714T>G (p.Leu905Arg)	rs387907449	0.00009
NM_001288772.2(PIK3C2G):c.3459G>A (p.Leu1153=)	rs375555307	0.00006
NM_001288772.2(PIK3C2G):c.2918T>C (p.Val973Ala)	rs387907453	0.00003
NM_001288772.2(PIK3C2G):c.3822C>A (p.Ser1274Arg)	rs387907451	0.00003
NM_001288772.2(PIK3C2G):c.2809A>T (p.Thr937Ser)	rs387907452
NM_001288772.2(PIK3C2G):c.3816A>G (p.Glu1272=)	rs387907450

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