rs3918242, MMP9

N. diseases: 54
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.
Spider nevus
CUI: C0085666
Disease: Spider nevus
2 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2017 2017
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019