rs147233090, CATSPER2P1

N. diseases: 6
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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2017 2017
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2019 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2016 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 0.700 1.000 1 2019 2019