Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs139974673
rs139974673
CATSPER2P1
15 43735687 intron variant T/C snv 2.0E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs139974673
rs139974673
CATSPER2P1
15 43735687 intron variant T/C snv 2.0E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2017 2017
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs147233090
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016