List of variants in gene PIK3R1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_181523.3(PIK3R1):c.514G>A (p.Val172Met)	rs112487959	0.00003
NM_181523.3(PIK3R1):c.811A>G (p.Met271Val)	rs761209777	0.00002
NM_181523.3(PIK3R1):c.1628G>A (p.Arg543Lys)	rs1367776221	0.00001
NM_181523.3(PIK3R1):c.1380_1397del (p.Ser460_Leu466delinsArg)	rs2531002229
NM_181523.3(PIK3R1):c.665T>C (p.Leu222Pro)

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