Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs560026225 1.000 0.080 4 122134546 intergenic variant -/AT delins 1.3E-02 1
rs71266076 1.000 0.080 8 80354702 intron variant -/C;TGAGACA ins 1.4E-05 1
rs202011557 1.000 0.080 2 102297182 intergenic variant -/CAA delins 1
rs113092121
KIF11
0.925 0.080 10 92624756 intron variant -/CTCT delins 2
rs149317277
ITGB8
0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36 2
rs11412402
EEFSEC
0.925 0.080 3 128194003 intron variant -/T ins 0.65 2
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs140522418
LOC107984408
0.925 0.080 11 128302942 intergenic variant A/-;AA delins 2
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs56267605 1.000 0.080 4 122441954 intergenic variant A/C snv 0.29 2
rs7183955
RORA
0.925 0.080 15 60757370 intron variant A/C snv 0.24 2
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 1
rs1012307
LINC01931 ; MMADHC-DT
1.000 0.080 2 149798707 intron variant A/C snv 4.9E-02 1
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 1
rs11635191
CCDC33
1.000 0.080 15 74257709 intron variant A/C snv 0.62 1
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 1
rs4673659
ERBB4
1.000 0.080 2 212325005 intron variant A/C snv 0.69 1
rs7305461 1.000 0.080 12 56056091 intergenic variant A/C snv 0.49 1