Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs2675669 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 1
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs12489120
BHLHE40 ; BHLHE40-AS1
1.000 0.040 3 4978778 intron variant C/A;G;T snv 1
rs2675662
CAMK2G
0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs4712528
CDKAL1
1.000 0.040 6 20678199 intron variant G/C;T snv 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2