rs10786156, PLCE1

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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 10 94254865 intron variant C/G snv 0.44 0.47 0.700 1.000 1 2019 2019
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 10 94254865 intron variant C/G snv 0.44 0.47 0.700 1.000 1 2016 2016