Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5