Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7921721
TBC1D12
10 94469762 intron variant C/T snv 0.45 1
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 3
rs74298199 7 93009803 intergenic variant A/G snv 5.9E-02 1
rs35183060
DIPK1A
1 92881371 intron variant A/G;T snv 1
rs73406759
CDK6
7 92719002 intron variant T/G snv 0.11 1
rs2488087 10 92686284 upstream gene variant G/A snv 0.42 1
rs42042
CDK6
7 92617798 intron variant C/A;G;T snv 2
rs12740
ANKIB1
7 92399988 3 prime UTR variant G/A snv 0.67 1
rs420271
LOC105369902
12 92369304 regulatory region variant A/G;T snv 1
rs11625753
PPP4R3A
14 91474797 non coding transcript exon variant T/C snv 0.20 1
rs13357230
LUCAT1 ; ADGRV1
5 91115255 intron variant A/G snv 5.8E-02 1
rs2184540
LOC100507103
9 91038926 intergenic variant G/A;T snv 0.19 1
rs2089111
LOC105369895 ; LINC02822
12 90786242 intron variant C/G snv 0.22 1
rs7908590
LARP4B
10 906583 intron variant C/G snv 4.7E-02 1
rs55771973
BACH2
6 90271600 intron variant T/A;G snv 1
rs10881645
KIF20B
10 89730330 intron variant A/G snv 0.49 1
rs4934494 10 89687662 intron variant G/A snv 0.22 1
rs2118193 16 89673495 intron variant G/A snv 0.24 1
rs140088599
ANKRD11
16 89374136 intron variant C/G snv 1.1E-02 1
rs73772144
MEF2C-AS1
5 89305735 intron variant G/A snv 6.5E-02 1
rs4842486
LINC02458
12 89238971 intron variant C/T snv 0.74 1
rs62045849 16 89038599 intergenic variant G/A snv 3.5E-02 1
rs7897395
FAS ; FAS-AS1
10 88994850 intron variant T/A;C snv 1
rs117473347 16 88990805 intron variant G/A snv 3.1E-02 1