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: rs183360145
rs183360145
CMAHP ; CARMIL1
6 25296893 intron variant T/C snv 2.6E-03
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2017 2017
dbSNP: rs183360145
rs183360145
CMAHP ; CARMIL1
6 25296893 intron variant T/C snv 2.6E-03
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2017 2017
dbSNP: rs116418977
rs116418977
CMAHP ; CARMIL1
6 25365660 intron variant C/T snv 4.8E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs62392365
rs62392365
CMAHP ; CARMIL1
1.000 0.040 6 25371141 intron variant A/T snv 3.2E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2019
dbSNP: rs62392365
rs62392365
CMAHP ; CARMIL1
1.000 0.040 6 25371141 intron variant A/T snv 3.2E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs111722075
rs111722075
CMAHP ; CARMIL1
6 25373818 intron variant C/T snv 0.11
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0.700 1.000 1 2017 2017
dbSNP: rs111722075
rs111722075
CMAHP ; CARMIL1
6 25373818 intron variant C/T snv 0.11
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		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: 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: rs2328887
rs2328887
CMAHP ; CARMIL1
6 25429921 intron variant T/C snv 0.91
CUI: C0005890
Disease: Body Height
Body Height 		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
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: 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: 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: 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