rs10036386, PDE8B

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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 1.000 0.040 5 77247778 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
thyroid function
CUI: C2242456
Disease: thyroid function
60 1.000 0.040 5 77247778 intron variant C/T snv 0.40 0.700 1.000 1 2012 2012