Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10460003
LINC01882
18 12747013 intron variant C/T snv 0.15 2
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10752747
MMEL1
1 2593476 intron variant G/T snv 0.41 2
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs11043097
LINC02752
11 11114248 intron variant T/C snv 0.15 2
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1194849
SPRED2
2 65379519 intron variant T/C snv 0.49 2
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs12138909
MMEL1
1 2607299 intron variant C/T snv 0.11 2
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5