rs2046045, PDE8B

N. diseases: 4
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 function
CUI: C2242456
Disease: thyroid function
60 0.925 0.080 5 77239986 intron variant T/C;G snv 0.800 1.000 1 2012 2012
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
27 0.925 0.080 5 77239986 intron variant T/C;G snv 0.700 1.000 1 2018 2018
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
83 0.925 0.080 5 77239986 intron variant T/C;G snv 0.700 1.000 1 2015 2015
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
10 0.925 0.080 5 77239986 intron variant T/C;G snv 0.010 1.000 1 2015 2015