Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs7617480
KLHDC8B
3 49173299 intron variant A/C snv 0.76 1
rs3914188
EEF1AKMT4-ECE2 ; ECE2
3 184292260 3 prime UTR variant G/C snv 0.73 0.73 1
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 1
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 1
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 1
rs6762477
RBM6
3 50055776 intron variant G/A snv 0.64 1
rs314273
LIN28B
6 105014007 intron variant T/G snv 0.64 1
rs167539
LIN28B
6 104962173 intron variant C/A snv 0.64 1
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs369065
LIN28B
6 104996183 intron variant C/T snv 0.63 1
rs6439371 3 132891908 intergenic variant G/A snv 0.63 1
rs900145 11 13272358 upstream gene variant C/T snv 0.62 1
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs2254479
USP49
6 41863405 intron variant G/A snv 0.62 1
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs2479724
BYSL
6 41923244 intron variant T/C snv 0.62 1
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs4693089
HELQ
4 83452469 intron variant A/G snv 0.60 1
rs4929923
TRIM66
11 8617653 3 prime UTR variant T/C snv 0.59 1
rs10441737
ZNF483
9 111539305 intron variant C/T snv 0.59 1
rs365132
UIMC1
5 176951573 synonymous variant G/T snv 0.51 0.58 1
rs852069
LOC105372544
20 17141948 intergenic variant A/G snv 0.57 1
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 1