rs13191659, LINC00240

N. diseases: 4
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.
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 6 27033276 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Iron binding capacity total measurement
CUI: C1283048
Disease: Iron binding capacity total measurement
35 6 27033276 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Total iron binding capacity function
CUI: C0700379
Disease: Total iron binding capacity function
35 6 27033276 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Transferrin saturation measurement
CUI: C1277709
Disease: Transferrin saturation measurement
36 6 27033276 intron variant C/G;T snv 0.700 1.000 1 2017 2017