rs13090803, None

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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 1.000 0.040 3 106216106 intron variant G/T snv 0.15 0.700 1.000 1 2019 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 1.000 0.040 3 106216106 intron variant G/T snv 0.15 0.700 1.000 1 2019 2019