rs5030772, FASLG

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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2013 2013
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2018 2018
Intervertebral Disc Degeneration
CUI: C0158266
Disease: Intervertebral Disc Degeneration
47 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2013 2013
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2018 2018
Squamous cell carcinoma of oropharynx
CUI: C0280313
Disease: Squamous cell carcinoma of oropharynx
33 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2015 2015
SVEINSSON CHORIORETINAL ATROPHY
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
30 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1 2020 2020