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: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7930786
rs7930786
11 116754011 intron variant C/G snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012