rs3219218, UNG

N. diseases: 4
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.
Carcinoma in situ of uterine cervix
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
18 0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 0.010 1 2018 2018
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 0.010 1.000 1 2018 2018
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 0.010 1.000 1 2018 2018
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 0.010 1 2014 2014