Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4236540
KPNA7
7 99171402 downstream gene variant G/T snv 0.68 1
rs59593577 11 95692362 intron variant C/T snv 0.12 1
rs12743520
EVI5
1.000 0.080 1 92571555 intron variant C/A snv 0.20 2
rs3540
IQGAP1
15 90502176 3 prime UTR variant G/A snv 0.43 2
rs2134814
BACH2
6 90277793 intron variant C/G snv 0.26 2
rs1612986 0.925 0.080 10 9022753 intergenic variant T/C snv 0.24 2
rs1444789 10 9022398 intergenic variant T/C snv 0.23 1
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1
rs1663687 1.000 0.080 10 9012824 intergenic variant G/A snv 0.35 1
rs962993 10 9011169 regulatory region variant C/T snv 0.34 1
rs1775550 10 9010779 regulatory region variant G/A;C snv 1
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 1
rs72782676 1.000 0.080 10 8990592 regulatory region variant C/G snv 5.1E-03 2
rs11255968 10 8894199 upstream gene variant C/T snv 9.3E-02 1
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs4908769
RERE
1 8641229 intron variant C/T snv 0.27 1
rs11255753 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 2
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs1409123 1.000 0.080 10 8540354 intergenic variant T/A snv 0.43 2
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29 2
rs13395467
LINC00299
1.000 0.120 2 8311368 intron variant A/G snv 0.24 1
rs367023
LINC00299
1.000 0.040 2 8309993 intron variant A/G snv 0.35 2