rs898275076, TG

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 3
CUI: C0342194
Disease: Thyroid Dyshormonogenesis 3
16 0.925 0.120 8 133022135 missense variant G/A snv 7.0E-06 0.700 0
Congenital Hypothyroidism
CUI: C0010308
Disease: Congenital Hypothyroidism
48 0.925 0.120 8 133022135 missense variant G/A snv 7.0E-06 0.010 1.000 1 2018 2018