rs9606756, TCN2

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.
Anemia, Pernicious
CUI: C0002892
Disease: Anemia, Pernicious
4 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2015 2015
Autoimmune gastritis
CUI: C3887639
Disease: Autoimmune gastritis
1 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2015 2015
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2017 2017
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2017 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2017 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2017 2017
Vitamin B 12 Deficiency
CUI: C0042847
Disease: Vitamin B 12 Deficiency
11 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2017 2017