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: rs2807278
rs2807278
ARG1
1.000 0.080 6 131488780 intron variant T/C snv 0.31
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2011 2011
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2491204
rs2491204
ARG1
6 131476264 intron variant T/A snv 0.75
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2014 2014
dbSNP: rs2608927
rs2608927
ARG1
6 131472903 intron variant T/A;C snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2014 2014
dbSNP: rs9321294
rs9321294
ARG1
6 131474417 intron variant T/C snv 0.75
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2014 2014