Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs7637230
LINC02085
0.925 0.040 3 101944711 intron variant A/G;T snv 2
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 2
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 2
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs7709212
LOC285626
0.925 0.040 5 159337169 intron variant T/C snv 0.34 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56 2
rs4712528
CDKAL1
1.000 0.040 6 20678199 intron variant G/C;T snv 1
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21 2
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11 6
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 1