Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs2248359
CYP24A1
0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 1
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 2
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 2
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 1
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 4
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2