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: rs11075253
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs115136538
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs115849089
rs115849089 		8 20054859 intergenic variant G/A snv 9.8E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs1168029
rs1168029
DOCK7
1 62503731 intron variant G/A;C snv
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs13247874
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2016
dbSNP: rs2575876
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs35853021
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs3764261
rs3764261 		0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs55791371
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs6065904
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2009 2012
dbSNP: rs651821
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs67418890
rs67418890 		1 161571067 intron variant T/A;C snv
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs6917603
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs7228085
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs72669744
rs72669744 		1 55650832 intron variant C/T snv 2.8E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs7412
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs2229738
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2012 2012