Source: GWASDB

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: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.810 0.500 1 2011 2013
dbSNP: rs9364554
rs9364554
SLC22A3
0.882 0.160 6 160412632 intron variant C/T snv 0.21
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.710 1.000 1 2008 2012
dbSNP: rs2048327
rs2048327
SLC22A3
0.851 0.120 6 160442500 intron variant T/C snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 3 2009 2014
dbSNP: rs12194182
rs12194182
SLC22A3
1.000 0.040 6 160413483 intron variant T/C snv 0.21
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 1.000 1 2012 2012
dbSNP: rs1567441
rs1567441
SLC22A3
6 160391230 intron variant T/C snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs376563
rs376563
SLC22A3
6 160430734 intron variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs9364554
rs9364554
SLC22A3
0.882 0.160 6 160412632 intron variant C/T snv 0.21
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010