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: 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: 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: 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: 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: 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: 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: 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