Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
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
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 6
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5