rs17185536, None

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
0.710 GeneticVariation GWASCAT In the discovery cohort, we identified a single locus (rs17185536-T) on chromosome 6 near the single-minded family basic helix-loop-helix transcription factor 1 (<i>SIM1</i>) gene that was significantly associated with the risk of erectile dysfunction (odds ratio = 1.26, <i>P</i> = 3.4 × 10<sup>-25</sup>). 30297428 2018
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
0.710 GeneticVariation BEFREE In the discovery cohort, we identified a single locus (rs17185536-T) on chromosome 6 near the single-minded family basic helix-loop-helix transcription factor 1 (<i>SIM1</i>) gene that was significantly associated with the risk of erectile dysfunction (odds ratio = 1.26, <i>P</i> = 3.4 × 10<sup>-25</sup>). 30297428 2018
Thyroxine measurement
CUI: C0202231
Disease: Thyroxine measurement
0.700 GeneticVariation GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018