rs57659670, 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.
Familial dyshormonogenetic goiter
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
5 0.925 0.120 15 45106240 missense variant T/C snv 9.8E-02 0.17 0.010 1.000 1 2011 2011
Subclinical hypothyroidism
CUI: C0271790
Disease: Subclinical hypothyroidism
10 0.925 0.120 15 45106240 missense variant T/C snv 9.8E-02 0.17 0.010 1.000 1 2011 2011