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: rs6657811
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2008 2019
dbSNP: rs6657811
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2019
dbSNP: rs6657811
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2008 2012