List of variants in gene PRKAG2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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.521C>T (p.Thr174Met)	rs148056866	0.00021
NM_016203.4(PRKAG2):c.1496A>G (p.Gln499Arg)	rs781741013	0.00012
NM_016203.4(PRKAG2):c.1304A>G (p.Asn435Ser)	rs200589374	0.00008
NM_016203.4(PRKAG2):c.356G>A (p.Arg119Gln)	rs142808871	0.00002
NM_016203.4(PRKAG2):c.320C>T (p.Pro107Leu)	rs730880985	0.00001
NM_016203.4(PRKAG2):c.1005+6T>C	rs1554464077
NM_016203.4(PRKAG2):c.358C>T (p.Arg120Cys)	rs763144065
NM_016203.4(PRKAG2):c.359G>A (p.Arg120His)	rs775756069
NM_016203.4(PRKAG2):c.452C>T (p.Ser151Phe)	rs1462809883
NM_016203.4(PRKAG2):c.590C>G (p.Pro197Arg)	rs368637364

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