Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 4
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 3