rs72709458, TERT

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.
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.882 0.040 5 1283640 intron variant C/A;T snv 0.700 1.000 1 2015 2015
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.882 0.040 5 1283640 intron variant C/A;T snv 0.700 1.000 1 2015 2015
Menorrhagia
CUI: C0025323
Disease: Menorrhagia
6 0.882 0.040 5 1283640 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.882 0.040 5 1283640 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.882 0.040 5 1283640 intron variant C/A;T snv 0.700 1.000 1 2019 2019