Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2255323 1.000 0.040 7 113078131 upstream gene variant C/T snv 0.17 1
rs240993
MFSD4B ; REV3L
1.000 0.040 6 111352511 intron variant T/A;C snv 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 1
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 1
rs3751385
GJB2
1.000 0.040 13 20188817 3 prime UTR variant A/G snv 0.74 1
rs3762999
TNIP1
1.000 0.040 5 151089865 intron variant C/T snv 0.49 1
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 1
rs4406273
LOC112267902 ; HLA-B ; LINC02571
0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02 1
rs465969
MFSD4B ; REV3L
1.000 0.040 6 111334327 intron variant G/A snv 8.7E-02 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs514315
SERPINB8
1.000 0.040 18 63989551 intron variant T/C snv 0.42 1
rs545979
POLI
1.000 0.040 18 54293380 intron variant C/T snv 0.26 1
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 1
rs6677595 1.000 0.040 1 152617711 downstream gene variant C/G;T snv 1
rs6809854
LOC105376976
1.000 0.040 3 18742931 intron variant A/G snv 0.19 1
rs7007032
CSMD1
1.000 0.040 8 3821924 intron variant C/T snv 0.75 1
rs7071642
ZNF365 ; LOC105378327
1.000 0.040 10 62654300 intron variant G/A snv 0.81 1
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 1
rs887466
POU5F1 ; PSORS1C3
1.000 0.040 6 31175734 intron variant G/A snv 0.40 1
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 1
rs9304742
ZNF816-ZNF321P
1.000 0.040 19 52948038 intron variant T/C snv 0.42 1
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44 1
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 1
rs953861
LOC285626
1.000 0.040 5 159345574 intron variant G/A;C snv 1