rs121909174, SLC5A5

N. diseases: 3
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 1
CUI: C1848805
Disease: Thyroid Dyshormonogenesis 1
7 0.925 0.120 19 17881961 missense variant A/C snv 1.2E-05 0.800 1.000 4 1997 1999
Iodide transport defect
CUI: C0271826
Disease: Iodide transport defect
2 0.925 0.120 19 17881961 missense variant A/C snv 1.2E-05 0.020 1.000 2 1998 2000
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.925 0.120 19 17881961 missense variant A/C snv 1.2E-05 0.010 1.000 1 1998 1998