List of variants in gene PRKAG2 reported as benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_016203.4(PRKAG2):c.*1061G>A	rs7429	0.54155
NM_016203.4(PRKAG2):c.*112A>G	rs8961	0.54129
NM_016203.4(PRKAG2):c.*522G>T	rs1051956	0.53580
NM_016203.4(PRKAG2):c.-26C>T	rs66628686	0.14343
NM_016203.4(PRKAG2):c.-90G>T	rs76351165	0.05040
NM_016203.4(PRKAG2):c.114+12C>T	rs77902041	0.04935
NM_016203.4(PRKAG2):c.1623T>C (p.Ile541=)	rs28763998	0.03936
NM_016203.4(PRKAG2):c.*452C>T	rs17714947	0.03769
NM_016203.4(PRKAG2):c.59G>T (p.Ser20Ile)	rs116605521	0.02188
NM_016203.4(PRKAG2):c.207G>A (p.Pro69=)	rs144384573	0.00538

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