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: rs17785382
rs17785382
LRP8 ; LOC100507564
1.000 0.040 1 53242281 intron variant A/G snv 0.31
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs2297661
rs2297661
LRP8 ; LOC105378728
1 53258293 intron variant C/G snv 2.9E-02 3.6E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5174
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5176
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012