Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 2
rs12445568
STX1B
0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 2
rs12602912
BPTF
1.000 0.040 17 67873957 intron variant C/G;T snv 2
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs2066819
STAT2
0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs2675662
CAMK2G
0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 2
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs4406273
LOC112267902 ; HLA-B ; LINC02571
0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02 2
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56 2
rs61871342
BLOC1S2
1.000 0.040 10 100278884 intron variant G/A snv 0.36 2
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 2
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 2
rs7637230
LINC02085
0.925 0.040 3 101944711 intron variant A/G;T snv 2
rs7709212
LOC285626
0.925 0.040 5 159337169 intron variant T/C snv 0.34 2
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 2
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10515778
LINC01932
1.000 0.040 5 159231004 intron variant A/G snv 0.13 1