Source: GWASCAT

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: rs4149310
rs4149310
9 104826853 intron variant A/T snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs4149310
rs4149310
9 104826853 intron variant A/T snv 0.34
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2012 2012
dbSNP: rs4149310
rs4149310
9 104826853 intron variant A/T snv 0.34
High density lipoprotein measurement
0.700 1.000 1 2018 2018