rs2046045, PDE8B

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
thyroid function
CUI: C2242456
Disease: thyroid function
0.800 GeneticVariation GWASCAT Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. 22494929 2012
thyroid function
CUI: C2242456
Disease: thyroid function
0.800 GeneticVariation GWASDB Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. 22494929 2012
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
0.700 GeneticVariation GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018
Thyroid stimulating hormone measurement
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
0.700 GeneticVariation GWASCAT Whole-genome sequence-based analysis of thyroid function. 25743335 2015
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
0.010 GeneticVariation BEFREE After adjusting for multiple testing by the program SNPSpD, allelic frequencies of rs4704397 (p = 0.016, OR = 1.692), rs6885099 (p = 0.031, OR = 0.621), and rs2046045 (p = 0.023, OR = 0.602) in PDE8B gene showed significant differences between patients with SCH and control subjects. 25822812 2015