Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6