List of variants in gene PRKAG2 reported as benign for Cardiovascular phenotype

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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.114+12C>T	rs77902041	0.04935
NM_016203.4(PRKAG2):c.1623T>C (p.Ile541=)	rs28763998	0.03936
NM_016203.4(PRKAG2):c.59G>T (p.Ser20Ile)	rs116605521	0.02188
NM_016203.4(PRKAG2):c.*3G>A	rs113234987	0.00973
NM_016203.4(PRKAG2):c.207G>A (p.Pro69=)	rs144384573	0.00538
NM_016203.4(PRKAG2):c.639C>T (p.Thr213=)	rs140001300	0.00493
NM_016203.4(PRKAG2):c.1296G>A (p.Thr432=)	rs114079815	0.00280
NM_016203.4(PRKAG2):c.1704G>A (p.Thr568=)	rs138167675	0.00150
NM_016203.4(PRKAG2):c.298G>A (p.Gly100Ser)	rs79474211	0.00144
NM_016203.4(PRKAG2):c.531G>T (p.Leu177=)	rs373000537	0.00001

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