Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10022109
TET2
4 105166665 intron variant A/G snv 0.20 1
rs10087240
PVT1
8 128000328 intron variant C/G;T snv 2
rs1014530
TRAF1
9 120922814 intron variant T/C snv 0.51 1
rs10243593 7 39932526 intergenic variant G/A snv 0.44 1
rs10401193
GATAD2A
19 19480257 intron variant A/G snv 0.19 1
rs10404046
EPS15L1
19 16366444 intron variant G/C snv 0.63 1
rs10408945
EPS15L1
19 16466180 intron variant G/T snv 0.14 1
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs10422126
MIR24-2 ; MIR27A ; MIR23A ; LOC284454
19 13837498 non coding transcript exon variant G/A snv 0.37 2
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs10554441
ETV1
7 13978399 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC delins 0.78 1
rs10554589
ANKRD11 ; LOC105371414
16 89295870 intron variant ATGTG/- delins 0.83 1
rs10828723
PRTFDC1
10 24916129 intron variant T/C snv 0.26 1
rs10844639 12 9736166 upstream gene variant C/T snv 0.31 1
rs10844706
CD69
12 9757536 intron variant C/A snv 0.34 1
rs10867411
TLE4
9 79683075 intron variant A/G snv 0.52 1
rs11077815
UBE2O
17 76393809 intron variant T/C;G snv 1
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs112158604 1 150724317 upstream gene variant GCTTCTGCA/- delins 1
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs11250079
PINX1
8 10815498 intron variant T/C snv 0.30 1
rs113678689
RBMS1
2 160450317 intron variant G/C;T snv 1
rs113924863 6 32615369 regulatory region variant C/T snv 1
rs116438126
HLA-B
6 31348683 intron variant C/T snv 9.0E-03 1