Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv 2
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 2
rs10168795
DOCK10
2 224888625 intron variant A/G snv 0.24 2
rs1021479 16 85923808 upstream gene variant T/A;C snv 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 2
rs1037171
CD300LF ; RAB37
17 74706839 intron variant G/A snv 0.53 2
rs10418046
NLRP12
19 53824615 upstream gene variant T/G snv 0.26 3
rs1042133
HLA-DPB1 ; HLA-DPA1
6 33080829 missense variant G/C snv 0.14 0.15 2
rs10489481 1 185422035 regulatory region variant G/A snv 0.31 2
rs10562650
ITGA4
2 181459460 intron variant TT/-;T;TTT delins 0.56 2
rs10751647
IFITM2
11 306884 upstream gene variant T/C snv 0.49 2
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv 2
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs10980800
LOC105376219
9 111153625 intron variant T/C snv 0.21 2
rs10987830 9 128016459 intergenic variant G/A snv 6.8E-03 2
rs1105527
KSR1
17 27521170 intron variant C/T snv 0.65 2
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs11189181
RRP12
10 97384397 intron variant A/G snv 0.30 2
rs11190141
LINC01475 ; NKX2-3
1.000 0.040 10 99532633 upstream gene variant C/T snv 0.40 3
rs112313229 3 46323369 intergenic variant G/A;T snv 2
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs112721625 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs113760175
CASC15
6 22343363 intron variant G/A;T snv 3
rs113899791
IRF8
16 85902784 5 prime UTR variant GGCTGCAGGT/-;GGCTGCAGGTGGCTGCAGGT;GGCTGCAGGTGGCTGCAGGTGGCTGCAGGT delins 2