rs267606976, PRKAG2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.080 7 151564203 missense variant A/G snv 0.700 1.000 2 2005 2014
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CUI: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
9 1.000 0.080 7 151564203 missense variant A/G snv 0.700 0