Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 2
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 2
rs7030641
CDKN2B-AS1
1.000 0.040 9 22054041 intron variant C/T snv 0.72 2
rs1360589
CDKN2B-AS1
1.000 0.040 9 22045318 intron variant C/T snv 0.72 2
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs7866783
CDKN2B-AS1
1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 2
rs1556515
CDKN2B-AS1
1.000 0.040 9 22036368 non coding transcript exon variant C/T snv 0.71 2
rs1008878
CDKN2B-AS1
1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 2
rs2069418
CDKN2B-AS1 ; CDKN2B
1.000 0.040 9 22009699 intron variant G/C snv 0.70 2
rs4451405
CDKN2B-AS1
9 22071751 intron variant C/T snv 0.69 1
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 1
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 3
rs712964 22 19168604 upstream gene variant T/C snv 0.66 1
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs7341791
CDKN2B-AS1
9 22112428 intron variant A/G snv 0.65 1
rs1537374
CDKN2B-AS1
1.000 0.040 9 22116047 intron variant A/G snv 0.64 2
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs7859362
CDKN2B-AS1
9 22105928 intron variant T/C snv 0.64 2