rs9257809, OR12D3;OR5V1

N. diseases: 10
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.
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.820 1.000 4 2012 2017
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2016 2016
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2007 2007
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.700 1.000 1 2016 2016
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.010 1.000 1 2013 2013
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.010 1.000 1 2017 2017
Heartburn
CUI: C0018834
Disease: Heartburn
5 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 0.010 1.000 1 2017 2017