Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849023 12 4223312 intergenic variant C/T snv 0.22 1
rs12135894 1 3811497 downstream gene variant C/A;T snv 1
rs218265 4 54542832 intergenic variant T/C snv 0.21 1
rs346522 19 43758393 upstream gene variant A/G snv 0.33 1
rs4916483 3 196180782 intergenic variant T/C snv 0.12 1
rs6092477 20 57416639 regulatory region variant G/A snv 0.36 1
rs6538148 12 88424702 intergenic variant C/G;T snv 1
rs7120391 11 5209677 downstream gene variant T/C snv 3.5E-02 1
rs718515 18 46276334 intergenic variant G/A snv 0.42 1
rs7221773 17 28875870 downstream gene variant G/A snv 0.15 1
rs737092 20 57415349 regulatory region variant T/C snv 0.58 1
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs6840258
AFF1
4 87052516 intron variant C/T snv 0.21 1
rs9683085
ATR
3 142529656 intron variant G/A snv 0.64 1
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 1
rs4890633
C18orf25
18 46253312 intron variant G/A snv 0.62 1
rs1790761
CABP4 ; GPR152
11 67454383 intron variant T/C snv 0.53 1
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22 1
rs2040494
CDK6
7 92627591 intron variant C/T snv 0.64 1
rs2572207
DENND4A ; RAB11A
15 65778355 intron variant C/A;T snv 1
rs9892942
FAM222B
17 28851743 intron variant C/T snv 0.25 1
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 1
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 1
rs9924561
FAM234A
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 1
rs11107
FBXO7
1.000 0.040 22 32479203 start lost G/A;C snv 0.45; 8.0E-06 1