Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 7
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 3
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 3
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
15 58434545 intron variant G/C snv 0.73 3
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 2
rs588136
ALDH1A2 ; LIPC ; LIPC-AS1
15 58438299 intron variant C/G;T snv 2
rs17269348
LIPC
0.925 0.040 15 58532442 intron variant A/G snv 7.8E-02 2
rs8034802
ALDH1A2 ; LIPC
15 58432593 intron variant T/A snv 0.33 1
rs11631342
ALDH1A2 ; LIPC
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 1
rs261336
ALDH1A2 ; LIPC ; LIPC-AS1
15 58450219 intron variant G/A snv 0.81 1
rs12914626
LIPC ; ALDH1A2 ; LIPC-AS1
1.000 0.040 15 58446224 intron variant C/T snv 0.54 1
rs7182229
LIPC ; LIPC-AS1 ; ALDH1A2
15 58472984 intron variant T/A;C;G snv 1