Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs4790694 0.882 0.160 17 4723059 downstream gene variant A/C snv 0.73 3
rs4522461
ARRB2
0.925 0.120 17 4718478 intron variant T/G snv 0.82 2
rs1131692181
CTNNB1
0.925 0.040 3 41234286 stop gained C/T snv 2
rs1375012922
DSG2
1.000 0.040 18 31538771 stop gained C/T snv 1