Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs10044254
FBXL7
0.925 0.080 5 15783487 intron variant A/G snv 0.25 1
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10175070
CCL20
1.000 0.080 2 227805859 5 prime UTR variant G/A;C snv 1
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs10836538
PRR5L
0.925 0.080 11 36343703 intron variant G/T snv 0.30 2
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs11000019
PSAP
1.000 0.080 10 71831773 intron variant G/A snv 3.3E-02 1
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs111789468
HLA-DPA1
1.000 0.080 6 33066047 non coding transcript exon variant C/T snv 0.21 1
rs111863753
GBA3
1.000 0.080 4 22794376 intron variant G/A snv 7.4E-03 2
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs113010607
SEPTIN8
0.925 0.080 5 132770006 intron variant T/C snv 0.21 2
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2