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: rs742132
rs742132
CARMIL1
0.925 0.120 6 25607343 intron variant A/G snv 0.29
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 1 2009 2009
dbSNP: rs75063949
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs75063949
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.700 1.000 1 2018 2018
dbSNP: rs13212936
rs13212936
CARMIL1
0.925 0.120 6 25588587 intron variant C/G;T snv 5.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs926326
rs926326
CARMIL1
6 25575174 intron variant A/C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs441460
rs441460
CARMIL1
6 25548060 intron variant G/A snv 0.45
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs12526480
rs12526480
CARMIL1
6 25533306 intron variant T/G snv 0.32
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6913974
rs6913974
CARMIL1
6 25528322 intron variant G/A snv 0.43
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs214053
rs214053
CARMIL1
6 25527735 intron variant T/C snv 0.43
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs214053
rs214053
CARMIL1
6 25527735 intron variant T/C snv 0.43
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs34164888
rs34164888
CARMIL1
6 25521693 intron variant C/A;T snv 0.19
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2019 2019
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2019 2019
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs35789010
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs202056061
rs202056061
CARMIL1
6 25494109 intron variant AGTT/- delins 2.8E-02
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		0.700 1.000 1 2017 2017
dbSNP: rs202056061
rs202056061
CARMIL1
6 25494109 intron variant AGTT/- delins 2.8E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0.700 1.000 1 2017 2017
dbSNP: rs34991172
rs34991172
CARMIL1
6 25480100 intron variant T/G snv 3.7E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs116272812
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs116272812
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs116272812
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs6918354
rs6918354
CMAHP ; CARMIL1
1.000 0.040 6 25444386 intron variant A/T snv 0.79
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019