List of variants in gene PRKAG2 reported as likely pathogenic for Hypertrophic cardiomyopathy

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016203.4(PRKAG2):c.1022T>C (p.Leu341Ser)	rs1563161306
NM_016203.4(PRKAG2):c.1030C>T (p.His344Tyr)	rs727504392
NM_016203.4(PRKAG2):c.1199C>A (p.Thr400Asn)	rs28938173
NM_016203.4(PRKAG2):c.1516G>C (p.Glu506Gln)	rs267606978
NM_016203.4(PRKAG2):c.1592G>T (p.Arg531Leu)	rs121908991
NM_016203.4(PRKAG2):c.967T>A (p.Phe323Ile)	rs397517283

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