rs6161, CYP11A1

N. diseases: 5
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.
Addison Disease
CUI: C0001403
Disease: Addison Disease
13 0.851 0.080 15 74343027 missense variant C/T snv 2.5E-03 2.6E-03 0.010 1.000 1 2019 2019
Adrenal cortical hypofunction
CUI: C0405580
Disease: Adrenal cortical hypofunction
5 0.851 0.080 15 74343027 missense variant C/T snv 2.5E-03 2.6E-03 0.010 1.000 1 2019 2019
Adrenal gland hypofunction
CUI: C0001623
Disease: Adrenal gland hypofunction
10 0.851 0.080 15 74343027 missense variant C/T snv 2.5E-03 2.6E-03 0.010 1.000 1 2019 2019
Adrenal Insufficiency, Congenital
CUI: C3502131
Disease: Adrenal Insufficiency, Congenital
1 0.851 0.080 15 74343027 missense variant C/T snv 2.5E-03 2.6E-03 0.010 1.000 1 2017 2017
Primary Adrenal Insufficiency
CUI: C3887896
Disease: Primary Adrenal Insufficiency
2 0.851 0.080 15 74343027 missense variant C/T snv 2.5E-03 2.6E-03 0.010 1.000 1 2019 2019