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: rs6987037
rs6987037
8 26819000 intron variant C/T snv 3.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6987037
rs6987037
8 26819000 intron variant C/T snv 3.0E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012