Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34976449
RERE
1 8438266 3 prime UTR variant -/G delins 0.66 1
rs59073566
LOC101928994
10 69215315 downstream gene variant -/T;TT delins 1
rs71973827
LOC105369568
11 128612542 downstream gene variant A/- delins 0.14 1
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs2224234 14 102915701 downstream gene variant A/C snv 0.33 1
rs4826685 X 3737519 intergenic variant A/C snv 0.34 1
rs6433895
LINC01934
2 181147287 intron variant A/C snv 0.31 1
rs6911302
RIPOR2
6 24819824 intron variant A/C snv 0.46 1
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs7192652
NLRC5
16 57041268 intron variant A/C;G snv 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs10022109
TET2
4 105166665 intron variant A/G snv 0.20 1
rs10401193
GATAD2A
19 19480257 intron variant A/G snv 0.19 1
rs10867411
TLE4
9 79683075 intron variant A/G snv 0.52 1
rs13182402
ALDH7A1
0.925 0.160 5 126582456 intron variant A/G snv 0.15 1
rs13315469
LOC105374216 ; TNIK
3 171142104 intron variant A/G snv 0.32 1
rs140397066
ARHGAP15
2 143404536 intron variant A/G snv 3.1E-03 1
rs1586459 4 38312549 intergenic variant A/G snv 0.85 1
rs1861090 12 9777083 intergenic variant A/G snv 0.34 1