rs6517135, OLIG2

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.
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.925 0.080 21 33025263 intron variant T/C snv 0.33 0.010 1.000 1 2019 2019
Hypoxic-Ischemic Encephalopathy
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
12 0.925 0.080 21 33025263 intron variant T/C snv 0.33 0.010 1.000 1 2019 2019