rs12621278, ITGA6

N. diseases: 7
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.
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.710 1.000 4 2009 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.710 1.000 2 2009 2010
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.700 1.000 1 2010 2010
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.010 1.000 1 2013 2013
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.010 1.000 1 2011 2011
melanoma
CUI: C0025202
Disease: melanoma
515 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.010 1.000 1 2011 2011
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.010 1.000 1 2011 2011