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: rs12801636
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2013 2018
dbSNP: rs12790427
rs12790427
PCNX3
11 65617256 synonymous variant C/G;T snv 1.7E-05; 0.25
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12790427
rs12790427
PCNX3
11 65617256 synonymous variant C/G;T snv 1.7E-05; 0.25
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12790427
rs12790427
PCNX3
11 65617256 synonymous variant C/G;T snv 1.7E-05; 0.25
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12801636
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs12801636
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs12801636
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs2004649
rs2004649
MAP3K11 ; PCNX3
11 65613445 synonymous variant G/A snv 0.42 0.36
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs61744384
rs61744384
PCNX3
1.000 0.040 11 65619907 synonymous variant T/A;G snv 0.45; 4.1E-06
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		0.700 1.000 1 2018 2018