rs1079418, PDE10A

N. diseases: 1
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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 1.000 0.040 6 165633546 intron variant A/G snv 0.32 0.700 1.000 2 2016 2019