List of variants in gene PSMG2 reported as benign for not provided

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020232.5(PSMG2):c.366A>G (p.Ser122=)	rs2302768	0.38520
NM_020232.5(PSMG2):c.407+13C>T	rs12965549	0.09100
NM_020232.5(PSMG2):c.537C>T (p.Ile179=)	rs78701021	0.00311
NM_020232.5(PSMG2):c.247A>G (p.Arg83Gly)	rs144450904	0.00267
NM_020232.5(PSMG2):c.191C>T (p.Thr64Ile)	rs115693908	0.00222
NM_020232.5(PSMG2):c.40G>A (p.Gly14Ser)	rs3809917	0.00177
NM_020232.5(PSMG2):c.703-7A>G	rs189904513	0.00100
NM_020232.5(PSMG2):c.181T>C (p.Tyr61His)	rs201114531	0.00080
NM_020232.5(PSMG2):c.539G>A (p.Arg180His)	rs76809309	0.00021
NM_020232.5(PSMG2):c.582-16T>A	rs199868112	0.00017
NM_020232.5(PSMG2):c.289-28C>A
NM_020232.5(PSMG2):c.408-11A>T

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