Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1411741
GPC5
1.000 0.080 13 92101599 intron variant A/G snv 0.98 1
rs7100433
ECHS1
10 133370298 intron variant T/C snv 0.98 3
rs1201324
LINC02336
1.000 0.080 13 89601725 intron variant A/G snv 0.98 1
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 1
rs3099627 1.000 0.080 1 11439331 intergenic variant A/G snv 0.98 1
rs495806
LIPC ; ALDH1A2
15 58426498 intron variant C/A snv 0.98 1
rs9322913 14 32900409 intergenic variant G/T snv 0.98 1
rs641299
DLGAP1
1.000 0.080 18 3544664 intron variant T/A snv 0.98 1
rs425820
NOS1AP
1 162323874 intron variant G/A snv 0.98 2
rs2321168
STARD13 ; STARD13-AS
13 33279354 non coding transcript exon variant G/A snv 0.98 4
rs3019619 11 62039499 intergenic variant T/A snv 0.98 1
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs2819368
LMOD1
1 201941435 intron variant C/T snv 0.98 2
rs2012237
LOC105374482 ; CLNK
0.925 0.120 4 10519597 intron variant G/T snv 0.98 2
rs7665423
CLNK ; LOC105374482
0.925 0.120 4 10518976 intron variant A/T snv 0.98 2
rs784416
CEP152
15 48720728 intron variant G/C snv 0.97 1
rs10001632
CLNK ; LOC105374482
0.925 0.120 4 10520247 intron variant A/C snv 0.97 2
rs10919021
NOS1AP
1 162265600 intron variant C/T snv 0.97 1
rs2756231
SORCS1
10 106706654 intron variant C/T snv 0.98 0.97 1
rs6834483
ARAP2
4 35981489 intron variant C/T snv 0.97 1
rs1901815
UGT1A10 ; UGT1A8
2 233663168 intron variant A/C;G snv 0.97 2
rs891142
CETP
16 56970065 intron variant T/C snv 0.97 1
rs453789
LOC105371789 ; HDAC5
17 44118647 intron variant A/C snv 0.97 1
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4
rs1257763 9 94131663 intron variant A/G snv 0.97 1