Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12585310 13 26954210 intergenic variant G/A snv 0.27 1
rs12720460
NOS2
17 27801261 intron variant ATTT/-;ATTTATTT;ATTTATTTATTT delins 1
rs1280165854
CRLF1
19 18596702 missense variant G/A snv 7.0E-06 1
rs1297258
LOC101927745
21 15434390 intron variant C/T snv 0.44 1
rs13069567
LOC107986051
3 169042362 downstream gene variant A/T snv 0.23 1
rs1343126
MAGI3
1 113586470 intron variant A/T snv 0.25 1
rs1388585 12 40137889 downstream gene variant G/A snv 0.95 1
rs1420098
IL18R1
2 102367819 splice region variant T/C snv 0.35 0.33 1
rs1426809883
ICAM1
19 10284797 missense variant G/A snv 1
rs149169037 7 20537675 intergenic variant G/A snv 5.5E-02 1
rs1648234
CSRP3-AS1
11 19308167 intron variant G/A snv 0.72 1
rs16953946
CDYL2
16 80751551 intron variant T/A;C snv 1
rs17000400 4 75251521 regulatory region variant C/T snv 0.12 1
rs17057051
PTK2B
8 27370037 intron variant A/G snv 0.28 1
rs17207042
CD226
18 69870115 intron variant T/C snv 0.40 1
rs17800987
ZNF300P1
5 150943866 non coding transcript exon variant A/G snv 0.14 0.13 1
rs200829864
TLR4
9 117704494 missense variant G/A;T snv 2.1E-05 1
rs201507031
KRT8
12 52897488 missense variant C/A snv 1.1E-04 1.7E-04 1
rs2034498
SCLT1
4 128971750 non coding transcript exon variant C/A;G;T snv 1
rs2153283
IPMK
10 58212538 intron variant C/A snv 0.34 1
rs2179070
TRAF3IP2-AS1 ; TRAF3IP2
6 111564549 intron variant T/C;G snv 1
rs2231884
FIBP ; CCDC85B
11 65889093 upstream gene variant C/T snv 0.16 1
rs2274351
SUFU ; ACTR1A
10 102504350 intron variant C/G;T snv 0.48 1
rs2279990
FOSL2
2 28413873 3 prime UTR variant A/G snv 0.41 1
rs2297559
ITLN1
1 160884736 intron variant G/A snv 0.66 1