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: rs2412710
rs2412710
CAPN3
15 42391589 intron variant G/A snv 3.6E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2010 2018
dbSNP: rs149698681
rs149698681
CAPN3
15 42359702 5 prime UTR variant G/C snv 1.2E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs149698681
rs149698681
CAPN3
15 42359702 5 prime UTR variant G/C snv 1.2E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs28364406
rs28364406
CAPN3 ; LOC105370794
15 42387225 intron variant C/T snv 1.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs28364406
rs28364406
CAPN3 ; LOC105370794
15 42387225 intron variant C/T snv 1.4E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs28364406
rs28364406
CAPN3 ; LOC105370794
15 42387225 intron variant C/T snv 1.4E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs56702977
rs56702977
CAPN3
15 42379110 intron variant G/A snv 0.16
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2016 2016
dbSNP: rs8026198
rs8026198
CAPN3
15 42361263 intron variant A/C;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2017 2017