Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1716983
ULK4
1.000 0.160 3 41922636 intron variant G/A;C;T snv 1
rs28581706
ULK4
1.000 0.160 3 41829905 intron variant A/C;T snv 1
rs62258655
ULK4
1.000 0.160 3 41890838 intron variant G/A snv 0.11 1
rs73081364
ULK4
1.000 0.160 3 41872124 intron variant G/A;C;T snv 1
rs10935070
TOPBP1
3 133623144 missense variant T/C;G snv 0.29; 4.0E-06 1
rs11921527
TF ; INHCAP
3 133722323 intron variant G/A;C snv 1
rs12639304
TF ; INHCAP
3 133722750 intron variant A/T snv 0.42 1
rs4525863
TF ; INHCAP
1.000 0.080 3 133717292 intron variant C/A snv 0.32 1
rs6439431
TF ; INHCAP
3 133729265 intron variant A/C snv 0.38 1
rs6775042
TF ; INHCAP
3 133723401 intron variant G/C;T snv 1
rs6782523
TF ; INHCAP
3 133720073 intron variant C/G;T snv 0.34 1
rs6787177
TF ; INHCAP
3 133731876 intron variant C/T snv 0.38 1
rs6796795
TF ; INHCAP
3 133747378 intron variant A/G snv 8.0E-02 1
rs7646118
TF ; INHCAP
3 133731195 intron variant C/G;T snv 1
rs8177178
TF ; INHCAP
0.925 0.080 3 133744428 intron variant G/A snv 0.33 1
rs8177197
TF ; INHCAP
3 133750686 intron variant G/A snv 0.27 1
rs8177213
TF ; INHCAP
3 133753383 intron variant A/C snv 0.25 1
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 3
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 1
rs1358024
TF
3 133765344 intron variant C/T snv 0.13 1
rs1525889
TF
3 133771189 intron variant A/C snv 0.29 1
rs1525892
TF
1.000 0.040 3 133765868 intron variant G/A;T snv 1
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 1
rs1799899
TF
1.000 0.080 3 133756968 missense variant G/A snv 5.2E-02 4.5E-02 1
rs2692695
TF
1.000 0.080 3 133766610 intron variant A/G snv 0.56 1