rs11066320, PTPN11

N. diseases: 5
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.
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.710 1.000 2 2012 2013
Corpuscular Hemoglobin Concentration Mean
4389 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2012 2012
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2012 2012
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2009 2009
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2019 2019