rs891835, CCDC26

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.
Glioma
CUI: C0017638
Disease: Glioma
353 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.810 1.000 3 2009 2019
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.700 1.000 1 2009 2009
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.700 1.000 1 2010 2010
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.020 1.000 2 2010 2014
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.851 0.120 8 129479506 intron variant T/G snv 0.17 0.020 1.000 2 2010 2014