rs181461079, DUOX2

N. diseases: 2
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.
Thyroid Dyshormonogenesis 6
CUI: C1846632
Disease: Thyroid Dyshormonogenesis 6
15 0.925 0.120 15 45103960 missense variant C/A;T snv 4.1E-04; 1.2E-04 0.700 1.000 4 2011 2017
Congenital Hypothyroidism
CUI: C0010308
Disease: Congenital Hypothyroidism
48 0.925 0.120 15 45103960 missense variant C/A;T snv 4.1E-04; 1.2E-04 0.020 1.000 2 2016 2016