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: rs1564348
rs1564348
SLC22A1
6 160157828 intron variant T/C snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2010 2019
dbSNP: rs1564348
rs1564348
SLC22A1
6 160157828 intron variant T/C snv 0.14
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2010 2019
dbSNP: rs1564348
rs1564348
SLC22A1
6 160157828 intron variant T/C snv 0.14
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs651164
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 2 2009 2011
dbSNP: rs651164
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs662138
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2011 2011
dbSNP: rs662138
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2011 2011
dbSNP: rs9295125
rs9295125
SLC22A1
1.000 0.040 6 160157239 intron variant G/T snv 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012