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: rs6413504
rs6413504
19 11131239 intron variant A/G snv 0.45 0.39
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6413504
rs6413504
19 11131239 intron variant A/G snv 0.45 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6413504
rs6413504
19 11131239 intron variant A/G snv 0.45 0.39
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012