Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34795510
AFF3
2 99992378 intron variant C/T snv 2.6E-02 1
rs56127672
AFF3
2 99988291 intron variant G/C snv 1.5E-02 1
rs13032879
AFF3
2 99986297 intron variant C/T snv 0.13 1
rs34506349
AFF3
2 99982264 intron variant G/A;C snv 1
rs34321437
AFF3
2 99960959 intron variant C/T snv 2.6E-02 1
rs13023088
AFF3
2 99959842 intron variant C/T snv 0.13 1
rs79785879
AFF3
2 99900176 intron variant T/C snv 1.5E-02 1
rs4148398
ABCC2
10 99832865 intron variant A/G snv 0.70 1
rs2043007
AFF3
2 99732211 intron variant C/G;T snv 1
rs7579187
AFF3
2 99725106 intron variant G/A snv 0.53 2
rs77179555
AFF3 ; LOC105373504
2 99692662 intron variant C/A;G snv 1
rs55779933
AFF3
2 99672640 intron variant C/T snv 2.5E-02 2.3E-02 1
rs62154466
AFF3
2 99575083 intron variant G/A snv 1.3E-02 1
rs115028891
EIF5B
2 99346967 intron variant T/G snv 1.2E-02 1
rs62153807
LYG2
2 99242816 intron variant C/G snv 1.2E-02 1
rs62156361
TSGA10
2 99062636 intron variant G/A snv 1.2E-02 1
rs9399012 6 99045073 intergenic variant C/T snv 9.3E-02 1
rs1901859 2 98973196 intergenic variant G/T snv 1.2E-02 1
rs3823036
POU3F2
6 98836656 3 prime UTR variant T/C snv 0.31 2
rs7769568 6 98817208 intergenic variant A/G snv 0.44 1
rs17800861
GRIN2A
16 9859815 intron variant T/A snv 7.5E-02 1
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs12196849 6 98342921 intron variant C/A snv 0.29 1
rs7758926 6 98337920 intron variant A/G snv 0.17 1
rs75477016 6 98333320 intron variant C/T snv 8.8E-02 1