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: rs2321168
rs2321168
13 33279354 non coding transcript exon variant G/A snv 0.98
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2321168
rs2321168
13 33279354 non coding transcript exon variant G/A snv 0.98
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2321168
rs2321168
13 33279354 non coding transcript exon variant G/A snv 0.98
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2321168
rs2321168
13 33279354 non coding transcript exon variant G/A snv 0.98
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2555592
rs2555592
13 33202766 intron variant T/G snv 4.3E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2555592
rs2555592
13 33202766 intron variant T/G snv 4.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2764627
rs2764627
0.925 0.040 13 33202941 intron variant C/T snv 5.0E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2764627
rs2764627
0.925 0.040 13 33202941 intron variant C/T snv 5.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012