Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs6914622
SASH1
0.851 0.040 6 148193165 regulatory region variant G/T snv 0.33 5
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4