rs4704397, PDE8B

N. diseases: 13
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 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.800 1.000 2 2008 2012
Blood thyroid stimulating hormone analysis
7 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.700 1.000 1 2008 2008
Thyroid stimulating hormone measurement
83 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.700 1.000 1 2008 2008
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
Hypothyroidism in pregnancy
CUI: C1997262
Disease: Hypothyroidism in pregnancy
1 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2009 2009
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
10 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2015 2015
Subclinical hypothyroidism
CUI: C0271790
Disease: Subclinical hypothyroidism
10 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2009 2009
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014