Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7003385
ANK1
8 41729232 intron variant T/A;C snv 1
rs9998941
FSTL5
4 161403710 intron variant G/A snv 0.27 1
rs2171209
SYTL3
6 158762530 intron variant T/C snv 0.78 1
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 1
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs10511701
CDKN2B-AS1
9 22112600 intron variant T/A;C snv 2
rs10733376
CDKN2B-AS1
1.000 0.080 9 22114470 intron variant G/C snv 0.64 2
rs10811644
CDKN2B-AS1
1.000 0.040 9 22025068 intron variant A/T snv 0.56 2
rs1333043
CDKN2B-AS1
9 22106732 intron variant T/A snv 0.64 2
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 2
rs1537374
CDKN2B-AS1
1.000 0.040 9 22116047 intron variant A/G snv 0.64 2
rs7035484
CDKN2B-AS1
1.000 0.040 9 22025241 intron variant C/G snv 0.56 2
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs7859362
CDKN2B-AS1
9 22105928 intron variant T/C snv 0.64 2
rs10738604
CDKN2B-AS1
1.000 0.040 9 22025494 intron variant G/A snv 0.29 3
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 3
rs10811647
CDKN2B-AS1
1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs615552
CDKN2B-AS1
0.925 0.120 9 22026078 intron variant T/C snv 0.29 3
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 4