rs2983514, PDE10A

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.
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.925 0.040 6 165636631 intron variant A/G snv 0.34 0.700 1.000 1 2018 2018
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.040 6 165636631 intron variant A/G snv 0.34 0.700 1.000 1 2018 2018