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: rs17132261
rs17132261
TMEM232
1.000 0.080 5 110672513 intron variant C/T snv 4.8E-02
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		0.800 1.000 1 2009 2009
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: rs89107
rs89107
SLC35F1
6 118256880 intron variant G/A snv 0.46
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		0.800 1.000 1 2009 2009