Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 28
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 12
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 11
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 8
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 7
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 7
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5