Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10033073
STX18-AS1 ; LOC101928279
4 4773674 intron variant A/G snv 0.32 1
rs10068717
NDFIP1
5 142115369 intron variant C/T snv 0.67 1
rs10074523
KIF3A
1.000 0.080 5 132724891 intron variant C/A snv 0.62 2
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 1
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 2
rs10178845
LINC00299
1.000 0.080 2 8303673 intron variant G/A snv 0.23 1
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 1
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 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
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 1
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 1
rs10486391
ITGB8
1.000 0.080 7 20336395 intron variant A/G snv 0.37 1
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 1
rs10497813
PLCL1
2 198049348 intron variant G/T snv 0.43 1
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 2
rs10663129
RASA2
3 141602994 intron variant -/CT delins 0.29 1
rs10760123
PHF19
9 120888256 intron variant T/A;G snv 1