List of variants in gene PRKAG2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_016203.4(PRKAG2):c.864+35_864+36insA	rs35348247	0.76395
NM_016203.4(PRKAG2):c.864+32G>T	rs200549512	0.00147
NM_016203.4(PRKAG2):c.250C>T (p.Arg84Trp)	rs61746358	0.00056
NM_016203.4(PRKAG2):c.1318C>T (p.His440Tyr)	rs201878539	0.00051
NM_016203.4(PRKAG2):c.1678+10T>C	rs369965019	0.00015
NM_016203.4(PRKAG2):c.594G>A (p.Pro198=)	rs397517276	0.00009
NM_016203.4(PRKAG2):c.147C>T (p.Asp49=)	rs761196275	0.00005
NM_016203.4(PRKAG2):c.312C>T (p.Thr104=)	rs397517268	0.00004
NM_016203.4(PRKAG2):c.945A>G (p.Val315=)	rs759393540	0.00003
NM_016203.4(PRKAG2):c.393C>T (p.Ser131=)	rs1057520352	0.00001
NM_016203.3(PRKAG2):c.-514G>T
NM_016203.4(PRKAG2):c.1006-9dup	rs775574266
NM_016203.4(PRKAG2):c.115-5C>T
NM_016203.4(PRKAG2):c.1233+7A>T
NM_016203.4(PRKAG2):c.1305C>T (p.Asn435=)
NM_016203.4(PRKAG2):c.466+45241A>C
NM_016203.4(PRKAG2):c.912G>A (p.Ala304=)	rs145029525

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