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: 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
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: rs7752195
rs7752195
CMAHP ; CARMIL1
1.000 0.040 6 25418866 intron variant T/C snv 0.93
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs7752195
rs7752195
CMAHP ; CARMIL1
1.000 0.040 6 25418866 intron variant T/C snv 0.93
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs7774567
rs7774567
CMAHP ; CARMIL1
1.000 0.040 6 25425298 intron variant A/C;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7774567
rs7774567
CMAHP ; CARMIL1
1.000 0.040 6 25425298 intron variant A/C;G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
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: 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