Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 1
rs2596573 1.000 0.080 6 31380153 upstream gene variant C/T snv 0.75 1
rs2747457 1.000 0.080 6 29688640 intergenic variant T/G snv 0.22 1
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 1
rs3129073 1.000 0.080 6 29648045 TF binding site variant A/G snv 0.16 1
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs7762933 1.000 0.080 6 31194743 upstream gene variant T/C snv 0.43 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 1
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 1
rs2956467
C12orf54
1.000 0.080 12 48459456 intergenic variant G/A;C snv 1
rs234709
CBS
0.827 0.200 21 43066854 intron variant C/T snv 1
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 1
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 1
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 1
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 1
rs7177514
CHRNA3
0.882 0.080 15 78615064 intron variant C/G;T snv 1
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 1
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1