Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 7
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6