Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 3
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 3
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 3
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs6959212 7 38088724 intergenic variant T/C;G snv 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 2
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 2
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 2
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 2
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50 2
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs2261033
PRRC2A
0.925 0.160 6 31635814 non coding transcript exon variant A/G snv 0.42 2