rs13107325, SLC39A8

N. diseases: 34
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.
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2018 2018
Smoking
CUI: C0037369
Disease: Smoking
765 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2017 2017
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
95 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2011 2011
Vital capacity
CUI: C0042834
Disease: Vital capacity
746 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.030 1.000 3 2016 2019
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.020 0.500 2 2018 2020
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.010 1.000 1 2016 2016
Precursor B-cell lymphoblastic leukemia
23 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.010 1.000 1 2018 2018