Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs13239597
TNPO3 ; TPI1P2
0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 1
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 1
rs2176082
PXK
0.925 0.080 3 58345459 intron variant G/A snv 0.36 1
rs2275247
KIAA0319L
0.925 0.080 1 35442850 intron variant T/C snv 0.26 1
rs3131917 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 1
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 1
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 1
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs3128930 0.925 0.120 6 33107889 upstream gene variant C/T snv 0.31 3
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs11860650
ITGAM
0.882 0.120 16 31315385 intron variant C/T snv 0.14 2
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25 2
rs2239689
TNXB
0.925 0.120 6 32062507 intron variant G/A snv 0.33 0.25 2
rs3894194
GSDMA
0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 2
rs4963128
PHRF1
0.882 0.120 11 589564 intron variant T/C snv 0.64 2
rs7774954
HLA-DQB2
0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 2
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 1
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 1
rs624988 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 1
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 1
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4