rs16936752, WNK2

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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.120 9 93301408 intron variant T/G snv 8.3E-02 0.700 1.000 1 2011 2011
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.925 0.120 9 93301408 intron variant T/G snv 8.3E-02 0.010 1.000 1 2010 2010