Disease: Dermatitis, Atopic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 3
rs176095
PBX2 ; GPSM3
0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 3
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 2