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: rs7910620
rs7910620
GRID1
10 86087202 intron variant C/G;T snv
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		0.800 1.000 1 2009 2009
dbSNP: rs10159528
rs10159528
GRID1
10 85725660 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10736336
rs10736336
GRID1
10 85720952 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10749528
rs10749528
GRID1
10 85701227 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11201944
rs11201944
GRID1
1.000 0.080 10 86211516 intron variant G/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 1.000 1 2010 2010
dbSNP: rs1880381
rs1880381
GRID1
0.882 0.120 10 85762211 intron variant C/T snv 4.2E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs4488140
rs4488140
GRID1
10 85695926 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013