Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs10830956 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 1
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 1
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 1
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 1
rs4416670 0.827 0.240 6 43982716 intergenic variant T/C snv 0.45 1
rs4922117 1.000 0.040 8 19995075 regulatory region variant T/A;C;G snv 0.25 1
rs5945326 0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25 1
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs16940170
ALDH1A2
1.000 0.040 15 58392083 intron variant G/A snv 0.15 1
rs495348
ALDH1A2
1.000 0.040 15 58395591 intron variant C/G snv 0.82 1
rs675
APOA4
1.000 0.040 11 116820959 missense variant T/A;C snv 0.15; 1.2E-03 1
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 1
rs1127065
CAMK2B
1.000 0.040 7 44220272 synonymous variant C/G;T snv 1.7E-02; 0.41 1
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 1
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs3816117
CETP
1.000 0.040 16 56962246 5 prime UTR variant T/C snv 0.52 1