rs7224296, LRRC37A2;NSF

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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.160 17 46722680 intron variant G/A snv 0.59 0.700 1.000 3 2009 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.882 0.160 17 46722680 intron variant G/A snv 0.59 0.700 1.000 1 2012 2012
Intelligence
CUI: C0021704
Disease: Intelligence
2093 0.882 0.160 17 46722680 intron variant G/A snv 0.59 0.700 1.000 1 2019 2019
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.882 0.160 17 46722680 intron variant G/A snv 0.59 0.010 1.000 1 2018 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.882 0.160 17 46722680 intron variant G/A snv 0.59 0.010 1.000 1 2018 2018