rs1939012, MMP8

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.
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 1.000 0.040 11 102724404 intron variant T/C snv 0.58 0.700 1.000 1 2014 2014
Vertigo
CUI: C0042571
Disease: Vertigo
35 1.000 0.040 11 102724404 intron variant T/C snv 0.58 0.010 1.000 1 2018 2018