Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 5
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4