Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169314
C12orf43
12 121005313 intron variant A/C;G snv 2
rs373579
FCGR2A
1 161513694 intron variant A/C;G snv 2
rs2235367
ZHX3
20 41201482 intron variant A/C;G snv 1
rs2980875 8 125469505 intron variant A/C;G;T snv 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 3
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 1
rs6456350
E2F3
6 20405308 intron variant A/C;G;T snv 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs67710536
RPS6
9 19376257 3 prime UTR variant A/C;T snv 0.12; 4.3E-06 0.20 2
rs7955221 12 100456972 intergenic variant A/C;T snv 2
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv 2
rs626913 8 60635935 non coding transcript exon variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14