rs4282438, COL11A2P1

N. diseases: 6
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.
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.800 1.000 1 2013 2013
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.730 1.000 4 2013 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.730 1.000 4 2013 2016
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.030 1.000 3 2014 2016
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.010 1.000 1 2018 2018
Infiltrating Cervical Carcinoma
CUI: C1334177
Disease: Infiltrating Cervical Carcinoma
13 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.010 1.000 1 2016 2016